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CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene
  1. M C J Jongmans1,
  2. R J Admiraal2,
  3. K P van der Donk1,
  4. L E L M Vissers1,
  5. A F Baas1,
  6. L Kapusta3,
  7. J M van Hagen4,
  8. D Donnai5,
  9. T J de Ravel6,
  10. J A Veltman1,
  11. A Geurts van Kessel1,
  12. B B A De Vries1,
  13. H G Brunner1,
  14. L H Hoefsloot1,
  15. C M A van Ravenswaaij1
  1. 1Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, the Netherlands
  2. 2Department of Otorhinolaryngology, Radboud University Nijmegen Medical Centre, Nijmegen, the Netherlands
  3. 3Children’s Heart Centre, Radboud University Nijmegen Medical Centre, Nijmegen, the Netherlands
  4. 4Department of Clinical Genetics and Human Genetics, VU University Medical Centre, Amsterdam, the Netherlands
  5. 5Academic Unit of Medical Genetics and Regional Genetics Service, St Mary’s Hospital, Manchester, UK
  6. 6Centre for Human Genetics, UZ Gasthuisberg, University of Leuven, Leuven, Belgium
  1. Correspondence to:
 C van Ravenswaaij
 Department of Human Genetics, Radboud University Nijmegen Medical Centre, PO Box 9101, 6500 HB Nijmegen, the Netherlands;c.vanravenswaaij{at}antrg.umcn.nl

Abstract

Background: CHARGE syndrome is a non-random clustering of congenital anomalies including coloboma, heart defects, choanal atresia, retarded growth and development, genital hypoplasia, ear anomalies, and deafness. A consistent feature in CHARGE syndrome is semicircular canal hypoplasia resulting in vestibular areflexia. Other commonly associated congenital anomalies are facial nerve palsy, cleft lip/palate, and tracheo-oesophageal fistula. Specific behavioural problems, including autistic-like behaviour, have been described. The CHD7 gene on chromosome 8q12.1 was recently discovered as a major gene involved in the aetiology of this syndrome.

Methods: The coding regions of CHD7 were screened for mutations in 107 index patients with clinical features suggestive of CHARGE syndrome. Clinical data of the mutation positive patients were sampled to study the phenotypic spectrum of mutations in the CHD7 gene.

Results: Mutations were identified in 69 patients. Here we describe the clinical features of 47 of these patients, including two sib pairs. Most mutations were unique and were scattered throughout the gene. All patients but one fulfilled the current diagnostic criteria for CHARGE syndrome. No genotype-phenotype correlations were apparent in this cohort, which is best demonstrated by the differences in clinical presentation in sib pairs with identical mutations. Somatic mosaicism was detected in the unaffected mother of a sib pair, supporting the existence of germline mosaicism.

Conclusions:CHD7 mutations account for the majority of the cases with CHARGE syndrome, with a broad clinical variability and without an obvious genotype-phenotype correlation. In one case evidence for germline mosaicism was provided.

  • CHARGE syndrome
  • CHD7
  • clinical spectrum

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Footnotes

  • Published Online First 14 October 2005

  • Competing interests: none declared

  • Informed consent: informed consent was obtained from all patients whose photographs are reproduced in this article

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