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Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness
  1. K Nozu1,
  2. T Inagaki2,
  3. X J Fu1,
  4. Y Nozu1,
  5. H Kaito1,
  6. K Kanda1,
  7. T Sekine3,
  8. T Igarashi3,
  9. K Nakanishi4,
  10. N Yoshikawa4,
  11. K Iijima5,
  12. M Matsuo1
  1. 1
    Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan
  2. 2
    Department of General Pediatrics, Miyagi Children’s Hospital, Ochiai, Aoba, Sendai Miyagi, Japan
  3. 3
    Department of Pediatrics, Graduate School of Medicine, The University of Tokyo, Japan
  4. 4
    Department of Pediatrics, Wakayama Medical University, Wakayama, Japan
  5. 5
    Department of Nephrology, National Center for Child Health and Development, Tokyo, Japan
  1. Dr K Nozu, Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe 650-0017, Kusunokicho 7-5-1, Chuo, Kobe, Hyogo, Japan; nozu{at}med.kobe-u.ac.jp

Abstract

Background: Bartter syndrome (BS) is a genetic disorder accompanied by hypokalaemic metabolic alkalosis. BS with sensorineural deafness (SND, OMIM602522) is a newly identified phenotype caused by mutations in the BSND gene that encodes barttin, a β-subunit for chloride channel ClC-Ka and ClC-Kb and classified as type IV BS. Type IV BS features the most severe phenotype entailing life-threatening neonatal volume depletion and chronic renal failure developing during infancy. A recent report described a case of BS with SND from a consanguineous family who showed homozygous mutations in the CLCNKA and CLCNKB genes. This case indicated the possibility of the occurrence of digenic inheritance in BS with SND resulting from double mutations in the CLCNKA and CLCNKB genes.

Subject and results: The current report concerns a 2-year-old girl from a non-consanguineous family with BS accompanied by SND. In our case, four loss-of-function mutations, consisting of mutations in both parental alleles in both CLCNKA and CLCNKB, were identified. The paternal allele had a nonsense mutation (Q260X) in CLCNKA and a splicing site mutation (IVS17+1 g>a) in CLCNKB. The maternal allele had a large deletion mutation (about 12 kbp) extending from CLCNKA to CLCNKB. Our case provides clear evidence that loss-of-function alleles in both alleles of both CLCNKA and CLCNKB results in a phenotype indistinguishable from that of mutations in BSND (type IV BS).

Conclusions: Recent advances in genetics have resulted in a better understanding of many human inherited diseases, but most of them are monogenic disorders and more complex inheritance patterns remain unresolved. Our case provides clear evidence of digenic inheritance outside the scope of Mendelian inheritance disorders.

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Footnotes

  • Funding: This study was supported by Grants from the Ministry of Education, Culture, Sports, Science and Technology of Japan.

  • Competing interests: None declared.

  • Patient consent: Parental/guardian informed consent was obtained for publication of the person’s details in this report.

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