Genetic testing for hearing loss in the United States should include deletion/duplication analysis for the deafness/infertility locus at 15q15.3

Nicole Hoppman, Umut Aypar, Pamela Brodersen, Neil Brown, Justin Wilson, Dusica Babovic-Vuksanovic

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

Background: Hearing loss is the most common birth defect and the most prevalent sensorineural disorder in developed countries. More than 50% of prelingual deafness is genetic, most often autosomal recessive and nonsyndromic, of which 50% can be attributed to the disorder DFNB1, caused by mutations in GJB2 and GJB6. Sensorineural hearing loss and male infertility (Deafness-Infertility Syndrome; DIS) is a contiguous gene deletion syndrome resulting from homozygous deletion of the CATSPER2 and STRC genes on chromosome 15q15.3. Females with DIS have only hearing loss and are fertile. Until recently this syndrome has only been described in three consanguineous families and 2 nonconsanguineous families. Results: We recently indentified a patient with hearing loss and macrocephaly who was found to be homozygous for this deletion. Her nonconsanguineous parents are both carriers. We examined our database of patients tested by array CGH and determined that just over 1% of our patients are heterozygous for this deletion. If this number is representative of the general population, this implies a 1% carrier frequency and prevalence of DIS of 1 in 40,000 individuals. Conclusion: We propose that DIS is a greatly under-diagnosed cause of deafness and should be considered in children with hearing loss. Likewise, current molecular genetic testing panels for hearing loss in the United States should be expanded to include deletion/duplication analysis of this region.

Original languageEnglish (US)
Article number19
JournalMolecular Cytogenetics
Volume6
Issue number1
DOIs
StatePublished - May 9 2013

Fingerprint

Genetic Testing
Audition
Deafness
Hearing Loss
Infertility
Testing
Megalencephaly
Genes
Sensorineural Hearing Loss
Male Infertility
Gene Deletion
Developed Countries
Chromosomes
Molecular Biology
Parents
Databases
Mutation
Defects
Population

Keywords

  • Array CGH
  • CATSPER2
  • Deafness-Infertility Syndrome
  • STRC

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Medicine
  • Molecular Biology
  • Genetics
  • Genetics(clinical)
  • Biochemistry, medical

Cite this

Genetic testing for hearing loss in the United States should include deletion/duplication analysis for the deafness/infertility locus at 15q15.3. / Hoppman, Nicole; Aypar, Umut; Brodersen, Pamela; Brown, Neil; Wilson, Justin; Babovic-Vuksanovic, Dusica.

In: Molecular Cytogenetics, Vol. 6, No. 1, 19, 09.05.2013.

Research output: Contribution to journalArticle

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