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Abstract
Background Congenital diaphragmatic hernia (CDH) is a life-threatening birth defect that often co-occurs with non-hernia-related anomalies (CDH+). While copy number variant (CNV) analysis is often employed as a diagnostic test for CDH+, clinical exome sequencing (ES) has not been universally adopted.
Methods We analysed a clinical database of ~12 000 test results to determine the diagnostic yields of ES in CDH+ and to identify new phenotypic expansions.
Results Among the 76 cases with an indication of CDH+, a molecular diagnosis was made in 28 cases for a diagnostic yield of 37% (28/76). A provisional diagnosis was made in seven other cases (9%; 7/76). Four individuals had a diagnosis of Kabuki syndrome caused by frameshift variants in KMT2D. Putatively deleterious variants in ALG12 and EP300 were each found in two individuals, supporting their role in CDH development. We also identified individuals with de novo pathogenic variants in FOXP1 and SMARCA4, and compound heterozygous pathogenic variants in BRCA2. The role of these genes in CDH development is supported by the expression of their mouse homologs in the developing diaphragm, their high CDH-specific pathogenicity scores generated using a previously validated algorithm for genome-scale knowledge synthesis and previously published case reports.
Conclusion We conclude that ES should be ordered in cases of CDH+ when a specific diagnosis is not suspected and CNV analyses are negative. Our results also provide evidence in favour of phenotypic expansions involving CDH for genes associated with ALG12-congenital disorder of glycosylation, Rubinstein-Taybi syndrome, Fanconi anaemia, Coffin-Siris syndrome and FOXP1-related disorders.
- congenital
- hereditary
- and neonatal diseases and abnormalities
- genetics
- medical
- genetic testing
- human genetics
- respiratory tract diseases
Data availability statement
All data relevant to the study are included in the article or uploaded as supplementary information. All variants that have not been previously published have also been submitted to the ClinVar database.
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- congenital
- hereditary
- and neonatal diseases and abnormalities
- genetics
- medical
- genetic testing
- human genetics
- respiratory tract diseases
Introduction
Congenital diaphragmatic hernia (CDH) is a life-threatening birth defect that affects approximately 1 in 4000 newborns.1 In approximately 40%–60% of cases, CDH occurs in conjunction with other non-hernia-related anomalies (CDH+).2 The mortality rate for newborns treated in surgical centres is approximately 30%, but this may be a significant underestimate due to pregnancy termination and postnatal mortality prior to transfer to a surgical centre.3 The mortality rate is particularly high in the 25%–40% of cases in which CDH co-occurs with congenital heart defects (CDH+/CHD).4 Among CDH survivors, chronic oxygen dependency, gastro-oesophageal reflux, poor growth and cognitive delay are common.5
A variety of chromosomal, genomic and single gene disorders are associated with an increased risk for developing CDH.6 In some of these disorders, CDH is a major clinical feature and is found in a high percentage of affected individuals. Examples of such disorders include Donnai-Barrow syndrome (MIM #222448, LRP2), microphthalmia, syndromic 9 (MIM #601186, STRA6) and cardiac-urogenital syndrome (MIM #618280, MYRF), also known as cardiac-urogenital-diaphragm-lung syndrome.7–10 In other disorders, CDH is not a major clinical feature but is found at a frequency that is higher than what would be expected by random chance. Examples of such disorders include Simpson-Golabi-Behmel syndrome, type 1 (MIM #312870, GPC3), focal dermal hypoplasia (MIM #305600, PORCN), also known as Goltz-Gorlin syndrome, and Marfan syndrome (MIM #154700, FBN1).11–13 Despite advances in our understanding of the genes that contribute to the development of CDH, the genetic variants that contribute to most cases of isolated CDH and CDH+ have not been identified.14
Array-based copy number variant (CNV) analysis and exome sequencing (ES) studies are routinely used to identify genetic alterations in individuals with more than one congenital anomaly, particularly in cases where a specific diagnosis is not clinically apparent. The diagnostic and clinical utility of array-based CNV analyses has been well established, and is clearly indicated, in individuals with CDH+.6 Although studies have shown that ES can be used to identify a molecular diagnosis in individuals with CDH+,7 14 15 ES has not been universally adopted as a diagnostic test for this disorder.
Here, we analyse a clinical database of ~12 000 test results to determine the diagnostic yields of ES in individuals with CDH+ and to identify new phenotypic expansions involving CDH.
Methods
Database analysis and clinical review
We searched coded information from a clinical database of ~12 000 individuals who were referred to Baylor Genetics for ES (accessed May 2019) for individuals with CDH or CDH+ based on phenotypes included in their test indications. Individuals with an indication of diaphragmatic eventration or an abnormality of the diaphragm and fetuses/newborns with an indication of a suspected CDH, diaphragmatic eventration or diaphragm abnormality, were also included. In this manuscript, we refer to all of these individuals as having CDH. Individuals whose diaphragmatic defect was described only as paralysis or atrophy in the setting of systemic muscular atrophy, or for whom a diagnosis was made using array-based CNV detection assays, were not included in this study.
Each reported variant was classified as pathogenic, likely pathogenic, a variant of unknown significance (VUS), likely benign or benign based on American College of Medical Genetics and Genomics standards for the interpretation of sequence variants using the most current information available publicly and in local databases (November 2020).16 The ES results of individuals with CDH had also been previously classified by clinical laboratory geneticists as solved, probably solved, possibly solved, partially solved or unsolved. All cases that were not considered unsolved were then independently reviewed by a clinical geneticist to determine if a definitive, probable, or provisional diagnosis could be made based on molecular findings and phenotypic information contained in the test identification. The designation ‘partially solved’ was retained as an indication that the diagnosis could only explain a distinct subset of the phenotypes included in the test indication.
A definitive diagnosis was made if the individual carried pathogenic variant(s) in a gene whose inheritance was consistent with a disorder associated with that gene, and the phenotypic data provided in the indication were suggestive of the disorder. A definitive diagnosis was also made if the case was previously published regardless of the variant designation made by the laboratory.
A probable diagnosis was made if one of the following criteria was met: (1) the individual carried a likely pathogenic variant in a gene associated with an autosomal dominant or X-linked disorder whose inheritance was consistent with that disorder, and the phenotypic data provided in the indication were suggestive of the disorder, (2) the individual carried a pathogenic variant and a likely pathogenic variant or VUS in trans or two likely pathogenic variants in trans, in a gene associated with an autosomal recessive disorder, and the phenotypic data provided in the indication were suggestive of the disorder, or (3) the individual was mosaic for a pathogenic or likely pathogenic variant in an autosomal dominant gene or an X-linked gene in a male, and the phenotypic data provided in the indication were suggestive of the disorder.
A provisional diagnosis was made if one of the following criteria was met: (1) the individual carried only a single pathogenic variant in a gene associated with an autosomal recessive disease, and the phenotypic data provided in the indication were suggestive of the disorder, (2) the individual carried two VUSs in trans or a likely pathogenic variant and a VUS in trans, in a gene associated with an autosomal recessive disease, and the phenotypic data provided in the indication were suggestive of the disorder, (3) the individual was a female who carried a heterozygous pathogenic variant in a gene associated with an X-linked disorder, and the phenotypic data provided in the indication were suggestive of the disorder, or (4) the individual carried a VUS(s) in a gene whose inheritance was consistent with a disorder associated with that gene, and the phenotypic data provided in the indication were suggestive of the disorder.
The number of cases with a definitive or probable molecular diagnosis was then divided by the total number of CDH+ cases to determine the diagnostic yield. This process was then repeated for isolated CDH cases, and CDH+ cases in which CHD was reported in the test indication with the exception of: (1) isolated patent foramen ovale and/or patent ductus arteriosus which may persist in the presence of pulmonary hypertension, (2) dextroposition which, in the setting of CDH, is most likely a secondary finding due to the intrusion of the abdominal viscera into the thorax, (3) dilated aorta in an individual with a definitive, probable or provisional diagnosis of a connective tissue disorder associated with aortic dilation, (4) isolated functional anomalies such as valve regurgitation, (5) isolated ventricular hypertrophy, or (6) cardiomyopathy.
Calculation of CDH frequency
For genes that were recurrently implicated in the development of CDH in our cohort, we searched coded information from a clinical ES database at Baylor Genetics to determine the frequency of CDH among all individuals in which the gene was suspected to contribute to phenotypes listed in the testing indication. Individuals in the database for whom no phenotypes were provided in the test indication were not included since it could not be determined whether they had CDH.
Human subjects research
This work was approved by the institutional review board of Baylor College of Medicine (protocol H-47546) and was conducted in accordance with the ethical standards of this institution’s committee on human research and international standards.
Literature and database searches
We searched for reports in which CDH candidate genes and/or their associated genetic disorders were mentioned in conjunction with key words such as diaphragm, diaphragmatic hernia, CDH or diaphragmatic eventration.
Genomic knowledge fusion
We have previously developed and validated a computational algorithm whose core function is to integrate large-scale genomic knowledge from various sources—Gene Ontology, Mouse Genome Informatics phenotype annotations, the Protein Interaction Network Analysis, the Kyoto Encyclopedia of Genes and Genomics molecular interaction network data and micro RNA (miRNA) targeting data, the GeneAtlas expression distribution and transcription factor binding and epigenetic histone modification data from the NIH Roadmap Epigenomics Mapping Consortium—to develop a phenotype-specific score that can be used to rank genes based on their similarity to a set of training genes known to cause that phenotype in humans and/or mice.17 We have previously used this algorithm to generate CDH-specific pathogenicity scores for all RefSeq genes.18 The CDH pathogenicity scores reported here represent the centile rank of each gene as compared with all other RefSeq genes.
Statistical analyses
For comparisons of the diagnostic yields between groups, two-tailed Fisher’s exact tests were performed using a 2×2 contingency table calculator available through GraphPad QuickCalcs (https://www.graphpad.com/quickcalcs/contingency1/). When defining the penetrance of CDH associated with genetic disorders, 95% confidence intervals (CIs) were calculated using a binomial ‘exact’ calculator available through the UCSF Clinical and Translational Science Institute (http://www.sample-size.net/confidence-interval-proportion/).
Results
Diagnostic yields of clinical ES
In a clinical database of approximately 12 000 individuals who were referred for ES, we identified 76 individuals with CDH+ based on phenotypes included in their test indications (table 1, online supplemental table S1). ES provided a definitive (n=19; 25%) or a probable (n=9; 12%) diagnosis in 28 individuals for a diagnostic yield of 37% (28/76). In addition, seven provisional diagnoses were made. If these were included, the diagnostic yield would be 46% (35/76).
Supplemental material
Individuals with CDH+ for whom a definitive, probable or provisional diagnosis was made by exome sequencing
In the subset of 37 individuals with CDH+/CHD, a definitive (n=9; 24%) or probable (n=3; 8%) diagnosis was made in 12 individuals for a diagnostic yield of 32% (12/37). In addition, three provisional diagnoses were made. If these were included, the diagnostic yield would be 41% (15/37).
In the same clinical database, we identified six patients with what appeared to be isolated CDH based on their test indications. Among these individuals, ES provided a diagnosis in only one individual for a diagnostic yield of 16.7% (1/6). This individual, Subject 36, carried a maternally inherited c.1396_1399dup, p.(Y467fs) pathogenic variant in ZFPM2, the gene associated with autosomal dominant diaphragmatic hernia 3 (MIM #610187). CDH associated with ZFPM2 haploinsufficiency is known to be incompletely penetrant,19 20 which provides an explanation of why the mother in this family was unaffected and yet this individual’s brother and sister both had CDH.
The diagnostic yields of ES were not statistically different between individuals with CDH+ (28/76) and the subset of individuals with CDH+/CHD (12/37) (p=0.68). The same is true between the diagnostic yields of individuals with CDH+ with (12/37) or without CHD (16/39) (p=0.48). Although the diagnostic yield of ES in CDH+ and CDH+/CHD cases were higher than that seen associated with isolated CDH (1/6), the isolated CDH sample size was too low to reach statistical significance (p=0.42 and p=0.65, respectively).
Recurrently altered genes
Variants in six genes were identified in more than one individual with CDH or CDH+ in our cohort. We identified four individuals, Subjects 18–21 (5.3%; 4/76), who carried frameshift variants in KMT2D, the gene associated with Kabuki syndrome 1 (MIM #147920). Subsequent to our initial analysis, a male with CDH, hypoplastic left heart, and posteriorly rotated ears was referred for ES and was found to carry a de novo c.7223dupT, p.(S2409Lfs*25) (NM_003482.3) pathogenic variant in KMT2D. We then searched the database to determine the frequency of CDH among all individuals in which KMT2D was suspected to contribute to phenotypes listed in the testing indication. We found the CDH penetrance to be 5/56 (8.9%; 95% CI 3% to 19.6%).
Three individuals, Subjects 1–3 (3/76; 3.9%), carried de novo pathogenic variants in ABL1, the gene associated with congenital heart defects and skeletal malformations syndrome (MIM #617602). Two of these individuals have been published previously.21 We found a total of nine individuals in the clinical database who carried ABL1 variants that were thought to contribute to phenotypes listed in the testing indication. This suggests that CDH is a relatively common finding in individuals with congenital heart defects and skeletal malformations syndrome (33%; 3/9), but this small number of cases is insufficient to generate a clear estimate of penetrance (CI 7.5% to 70.1%).
Similarly, two individuals, Subjects 25 and 26 (2/76; 2.6%), whose cases were previously published, carried pathogenic variants in MYRF, the gene associated with cardiac-urogenital syndrome (MIM #618280).7 8 Subsequent to our initial analysis, a male with CDH, dextrocardia, hypoplastic left heart syndrome, pulmonary vein stenosis, a bifid scrotum, cryptorchidism and hypospadias was identified who carried a non-maternally inherited c.2057G>A, p.(R686H) (NM_013279.4) VUS in MYRF. Including this individual, 75% (3/4) of individuals in our database who carried putatively causative MYRF variants had CDH. This suggests that CDH is commonly seen in individuals with cardiac-urogenital syndrome, but this small number of cases is insufficient to generate a clear estimate of penetrance (95% CI 19.4% to 99.4%).
As previously mentioned, Subject 36 was found to carry a maternally inherited pathogenic variant in ZFPM2. A second individual, Subject 35, with both CDH and a sinus venosus atrial septal defect (CDH+/CHD), was also found to carry a heterozygous pathogenic variant in ZFPM2, consistent with this gene’s known function in cardiac development.22 23 In our database, we found one other individual with tetralogy of Fallot who carried a pathogenic variant in ZFPM2. Identification of CDH in 66% (2/3) of individuals in our database is consistent with a relatively high CDH penetrance, but this small number of cases is insufficient to generate a clear estimate of penetrance (95% CI 9.4% to 99.2%). We also note that ZFMP2-related disorders are associated with incomplete penetrance.
Two individuals, Subjects 11 and 12 (2/77; 2.6%), were found to carry heterozygous variants in EP300, the gene associated with Rubinstein-Taybi syndrome 2 (MIM #613684). The first carried a de novo, mosaic (12%) pathogenic EP300 variant. The second was a female who carried a c.3592T>C, p.(Y1198H) VUS in EP300 and also carried a c.3298G>T, p.(D1100Y) VUS in SOS1, the gene associated with autosomal dominant, Noonan syndrome 4 (MIM #610733) and a heterozygous, pathogenic c.-142C>G, p.? variant in DKC1, the gene associated with dyskeratosis congenita, X-linked (MIM #305000). The inheritance pattern of these variants could not be determined due to a lack of parental samples, and the phenotypes provided in the indication are not sufficient to clearly delineate which of these variants, alone or in combination, are contributing to her symptoms. A total of 20 individuals in the clinical database carried EP300 variants that were thought to contribute to phenotypes listed in the testing indication. This suggests that CDH occurs in a low percentage of individuals with Rubinstein-Taybi syndrome 2 (10%; 95% CI 1.2% to 31.7%).
Two individuals, Subjects 5 and 6 (2/76; 2.6%), were found to carry compound heterozygous pathogenic variants in ALG12, the gene associated with ALG12-congenital disorder of glycosylation (ALG12-CDG, formerly CDG Ig; MIM #607143).24 These individuals were the only ones in the clinical database (2/2, 100%) in which ALG12 variants in trans were thought to contribute to phenotypes listed in the testing indication.
Other novel candidate genes for CDH
Among the 76 individuals with CDH+, several carried putatively deleterious variants in genes that are clearly associated with an increased risk of developing CDH including ABL1, B3GALT6, FBN1, HCCS, KMT2D, LRP2, MRYF, POGZ, SLC2A10 and ZFPM2.7 21 The remainder carried putatively deleterious variants in genes whose association with CDH has not been clearly established (online supplemental table S1). To determine if deleterious variants in these genes were likely to be associated with the development of CDH, we determined whether each gene is expressed in the developing mouse diaphragm at embryonic day (E)11.5, E12.5 and E16.5 based on whole-transcriptome expression profiles published by Russell et al.25 We then determined if these genes were associated with high CDH-specific pathogenicity scores (≥85% based on all RefSeq genes) previously generated using a validated genome-scale knowledge fusion algorithm.17 18 We also performed a literature review to identify reports in which these genes, or their corresponding syndromes, have been previously linked to CDH. Based on these data, we determined which candidate genes, or their associated syndromes, had sufficient evidence to support a phenotypic expansion including CDH (table 2) and which, currently, did not (table 3).
Candidate genes for which there is sufficient evidence to support a phenotypic expansion involving CDH
Candidate genes for which there is currently insufficient evidence to support a phenotypic expansion involving CDH
Discussion
The use of clinical ES has been shown to change medical management and genetic counselling regardless of testing outcome.26 27 The diagnosis of a specific genetic syndrome may reveal the need to address medical problems or risks that may not have been recognised prior to the diagnosis and can help to reduce medical waste by minimising the use of tests, imaging studies and medical interventions that are unlikely to provide significant benefit. ES also has the potential to identify novel genes that cause medically important phenotypes including CDH.7 14 15 Despite these benefits, ES has not been universally adopted as a diagnostic test in individuals with CDH+. This may be due to uncertainty regarding the diagnostic yield of clinical ES in these cases.
The high diagnostic yields of clinical ES in CDH+
Using information from a clinical database, we estimated the diagnostic yield of ES in individuals with CDH+. Among the 76 individuals with CDH+ in the database, ES was able to identify a diagnosis in 28 individuals for a diagnostic yield of 37% (28/76). In the subset of 37 individuals with CDH+/CHD, a diagnosis was made in 12 individuals for a diagnostic yield of 32% (12/37). This suggests that clinical ES can be used to identify a molecular diagnosis in a significant percentage of individuals with CDH+.
Although the diagnostic yield of clinical ES in CDH+ cases was not statistically different than the 16.7% (1/6) diagnostic yield seen in individuals with isolated CDH (p=0.42), we note that the number of isolated CDH cases in the database was too low to allow us to confidently estimate the diagnostic yield in this population (CI 0.4% to 64.1%). We also note that Subject 36, the only individual with isolated CDH who was positive on ES, has a positive family history of CDH in a brother and sisters.
CDH is a relatively common phenotype associated with Kabuki syndrome 1
Four individuals, Subjects 18–21, carried frameshift variants in KMT2D, the gene associated with Kabuki syndrome 1 (MIM #147920). This represented 5% (4/76) of our CDH+ cohort and 14% (4/28) of the subset of individuals with a molecular diagnosis. After completing our initial analysis, we identified a fifth patient with CDH+ who carried a KMT2D frameshift variant. By reviewing all cases in our clinical database, we estimated the CDH penetrance in Kabuki syndrome 1 to be 8.9% (5/56; CI 3% to 19.6%). In contrast, no individuals with CDH+ were found to carry putatively causative variants in KDM6A, the gene associated with Kabuki syndrome 2 (MIM #300867).
Phenotypic expansions involving CDH
Phenotypes with relatively high penetrance levels are easily identified using small cohorts of affected individuals. As penetrance drops, larger cohorts are needed to conclude that a phenotype is associated with a disorder based on clinical descriptions alone. Here, we seek to identify known human disease genes that contribute to the development of CDH but have previously escaped detection due to their low levels of CDH penetrance. In attempting to do so, we recognise that CDH is a relatively common birth defect with an incidence of approximately 1 in 4000 newborns.1 As a result, the CDH seen in some of the individuals in this cohort may not be associated with the variants we identified by clinical ES. Instead, such cases could represent single or dual diagnoses in which the causative pathogenic variant was not discovered by ES, or cases in which CDH was associated with a multifactorial inheritance pattern in which a variety of genetic, environmental, and stochastic factors lead to abnormal diaphragm development.
To distinguish which genes harbouring putatively pathogenic variants were more likely to be associated with the development of CDH, we determined how frequently variants in these genes were seen in our cohort, if the mouse homologs of these genes have been shown to be expressed in the developing mouse diaphragm,25 if these genes had high CDH-specific pathogenicity scores (≥85%),17 18 and whether there was additional evidence in the literature to support the association of these genes—or their corresponding genetic disorders—with CDH. Evidence in favour of a phenotypic expansion involving CDH was highest for: ALG12, EP300, BRCA2, FOXP1 and SMARCA4 (table 1).
We identified two fetuses, Subjects 5 and 6, which had CDH+ associated with diagnoses of ALG12-CDG (MIM #607143). This disorder is characterised by neurodevelopmental phenotypes and a variety of structural birth defects involving the brain, heart, genitourinary system and skeleton and is commonly lethal in the newborn period.24 Although ALG12 has a relatively low CDH-specific pathogenicity score (48.2%), its mouse homologue is expressed in the developing mouse diaphragm. Based on these findings, we conclude that CDH is a feature of ALG12-CDG.
Rubinstein-Taybi syndrome can be caused by autosomaldominant, pathogenic variants in CREBBP (type 1; MIM #180849) or EP300 (type 2; MIM #613684) and is characterised by neurodevelopmental phenotypes, distinct facial features, broad thumbs and first toes, short stature and a high rate of CHD and renal anomalies.28 Benjamin et al reported a possible association between CDH and Rubinstein-Taybi syndrome prior to the discovery of the genes that cause this disorder.29 We identified two individuals, Subjects 11 and 12, with variants in EP300 but none in CREBBP. Subject 12 also carried a pathogenic variant in DKC1, the gene associated with dyskeratosis congenita, X-linked (MIM #305000), and a VUS in SOS1, the gene associated with Noonan syndrome 4 (MIM #610733). It is possible that these variants contributed to the development of CDH in this individual, particularly since CDH has been previously documented in individuals with Noonan syndrome.7 30 31 We note that the mouse homologs of EP300 and CREBBP are expressed in the developing mouse diaphragm25 and have high CDH-specific pathogenicity scores (94.7% and 91.6%, respectively). This leads us to conclude that CDH is a phenotype that can be associated with Rubinstein-Taybi syndrome, particularly Rubinstein-Taybi syndrome 2, which is caused by pathogenic variants in EP300.
Fanconi anaemia is a genetically heterogeneous bone marrow failure syndrome associated with an increased risk for cancer and a variety of structural birth defects.32 We identified two individuals, Subjects 9 and 13, with CDH+ who carried changes in Fanconi anaemia genes. Subject 9 had a definitive diagnosis of Fanconi anaemia, complementation group D1 (MIM #605724) caused by compound heterozygous, pathogenic variants in BRCA2. The family history of this individual was positive for a paternal aunt with breast cancer and maternal great-grandmother with pancreatic cancer. This is consistent with transmission of heterozygous, pathogenic BRCA2 variants and a diagnosis of autosomal-dominant BRCA2-associated hereditary breast and ovarian cancer syndrome (MIM #612555, #613347) on both sides of the family. Subject 13 had a provisional diagnosis of Fanconi anaemia, complementation group I (MIM #609053) and phenotypes suggestive of this disorder. However, only a single pathogenic variant in FANCI was identified.
The mouse homologues of BRCA2 and FANCI are expressed in the developing mouse diaphragm,25 and CDH has been reported in at least one other individual who was clinically diagnosed with Fanconi anaemia.33 BRCA2 had a high CDH-specific pathogenicity score of 88.8%, while FANCI’s was much lower at 25%. These results lead us to conclude that CDH is a phenotype that can be associated with Fanconi anaemia, particularly Fanconi anaemia, complementation group D1, which is caused by biallelic pathogenic variants in BRCA2. In contrast, our results do not provide any evidence that individuals who carry a single pathogenic variant in BRCA2—or other genes that cause autosomal recessive forms of Fanconi anaemia—have an increased risk of developing CDH.
Coffin-Siris syndrome is a genetically heterogeneous disorder characterised by neurodevelopmental phenotypes, distinctive facial features, hypoplasia of the distal phalanx or nail of the fifth digits and congenital anomalies involving the central nervous, cardiac, gastrointestinal and genitourinary systems.34 Subject 31 had a definitive diagnosis of Coffin-Siris syndrome 4 (MIM #614609) caused by a pathogenic variant in SMARCA4. Subject 32 had a provisional diagnosis of Coffin-Siris syndrome 8 (MIM #618362) and carried a splice junction variant in SMARCC2. Previous reports have suggested that Coffin-Siris syndrome is associated with an increased risk of CDH.35–37 However, a specific association between CDH and SMARCA4 and SMARCC2 has not been suggested previously. The homologues of these genes are expressed in the developing mouse diaphragm and both have high CDH-specific pathogenicity scores of 93.7% and 89.9%, respectively. This leads us to conclude that CDH is a phenotype that can be associated with Coffin-Siris syndrome, particularly Coffin-Siris syndrome 4 caused by pathogenic variants in SMARCA4.
Pathogenic variants in FOXP1 have been shown to cause mental retardation with language impairment and with or without autistic features (MIM #613670), a genetic disorder characterised by neurodevelopmental phenotypes, dysmorphic features, and congenital anomalies of the kidney and urinary tract.38 39 Subject 16 had a definitive diagnosis of mental retardation with language impairment and with or without autistic features. At least one other individual with CDH associated with a FOXP1 variant has been published previously.7 The mouse homologue of FOXP1 is expressed in the developing diaphragm, and FOXP1 has a CDH-specific pathogenicity score of 96.9%. This leads us to conclude that CDH is a phenotype that can be associated with mental retardation with language impairment and with or without autistic features.
Putatively pathogenic variants in ANKRD11, FOXC2, MED12, MCPH1, RASA1 and TCF12 were identified in one individual with CDH+. The mouse homologues of these genes are expressed in the developing diaphragm and all have CDH-specific pathogenicity scores ≥80%. Although these findings provide some evidence that deleterious variants in these genes may predispose to the development of CDH, we feel that the data at hand are insufficient to allow us to conclude that CDH is a phenotype that can be associated with their respective genetic disorders. Additional evidence for an association may come from the publication of more human cases or evidence of diaphragmatic defects in transgenic mouse models. Experience suggests that dedicated diaphragm studies may be needed to identify CDH in existing mouse models due to early lethality and incomplete penetrance which can vary based on genetic background.40–43
Study limitations
This study was based on coded data available from a clinical database. As such, we recognise several limitations. First, this is a retrospective study on a subset of patients with CDH+ referred for clinical ES. As a result, it is possible that our cohort may represent a selected population of individuals with CDH+ in which there was a higher likelihood of an underlying genetic diagnosis. This type of selection bias would tend to inflate the diagnostic yield. At the same time, individuals with CDH+ for whom a genetic diagnosis could have been made by clinical ES may not have been referred since a molecular diagnosis was made using single gene or panel testing. The exclusion of these individuals from our cohort would tend to lower the diagnostic yield. With this in mind, we would suggest that future studies aimed at confirming the results obtained here be conducted in a prospective manner in which clinical ES is ordered on all individuals presenting with CDH+, or on all individuals with CDH+ for whom array-based CNV analysis was negative.
The second limitation of this study is our inability to access additional clinical and molecular information on individuals in our cohort. As a result, we cannot indicate what percentage of individuals in our cohort underwent a chromosome analysis, array-based CNV analysis or targeted molecular testing. We are also unable to access information that might have allowed us to confirm or refute a particular diagnosis. This lack of information is unlikely to be of great importance with regard to individuals who received a definitive diagnosis based on their ES results but may have allowed us to reclassify individuals who received a probable or provisional diagnosis. This limitation could be minimised in a prospective study in which researchers have full access to medical records.
Recommendations for clinical practice
Given the high diagnostic yield of clinical ES we identified in our cohort of individuals with CDH+ (37%; 28/76), we conclude that ES should be ordered in cases of CDH+ when a specific diagnosis is not suspected and CNV analyses are negative. Physicians and surgeons should also consider ordering clinical ES in cases of isolated CDH in which there is a positive family history. We also conclude that CDH is a relatively common phenotype associated with Kabuki syndrome 1, and that CDH may be a phenotype associated with ALG12-congenital disorder of glycosylation, Rubinstein-Taybi syndrome, Fanconi anaemia, Coffin-Siris syndrome and FOXP1-related disorders. With this in mind, physicians should not discount the possibility that a patient has one of these diagnoses based on their also having CDH.
Data availability statement
All data relevant to the study are included in the article or uploaded as supplementary information. All variants that have not been previously published have also been submitted to the ClinVar database.
Ethics statements
Patient consent for publication
References
Supplementary materials
Supplementary Data
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Footnotes
Contributors CAS and DAS conceived and directed the study. SRL, PL and JAR provided molecular and clinical data. IMC and CAS performed the machine learning analysis. PL classified variants. DAS determined the level of diagnostic certainty. TMS, AH-G and DAS analysed the data. TMS and DAS wrote the manuscript. All authors reviewed, revised and approved the manuscript.
Funding This research was funded in part by NIH/NICHD grant HD098458 to DAS.
Competing interests The Department of Molecular and Human Genetics at Baylor College of Medicine derives revenue from the clinical ES performed at Baylor Genetics.
Provenance and peer review Not commissioned; externally peer reviewed.
Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.