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Results 1 - 10 of 14 for Hearing "loss," autosomal dominant 78
  1. Keratitis-ichthyosis-deafness syndrome 
    ... recessive keratitis-ichthyosis-deafness syndrome Genetic Testing Registry: Autosomal dominant keratitis-ichthyosis-hearing loss syndrome Keratitis-ichthyosis-deafness syndrome, autosomal recessive KID ...
    https://medlineplus.gov/.../keratitis-ichthyosis-deafness-syndrome - Genetics
  2. Palmoplantar keratoderma with deafness 
    ... Prera E, Schild C, Aschendorff A, Arndt S. Autosomal dominant prelingual hearing loss with palmoplantar keratoderma syndrome: Variability in clinical expression ...
    https://medlineplus.gov/.../palmoplantar-keratoderma-with-deafness - Genetics
  3. GJB2 gene 
    ... needed for hearing.DFNA3 is inherited in an autosomal dominant pattern, which means only one mutated copy of the GJB2 gene in each cell is sufficient to cause the condition. This form of hearing loss can be either prelingual or begin after a ...
    https://medlineplus.gov/genetics/gene/gjb2 - Genetics
  4. MYH9-related disorder 
    ... no history of the disorder in their family. Autosomal dominant MYH9 ... MYH9-related disease National Organization for Rare Disorders ( ...
    https://medlineplus.gov/genetics/condition/myh9-related-disorder - Genetics
  5. COL4A4 gene 
    ... Variants in this gene can also lead to hearing loss and changes in the lens of ... dominant Alport syndrome. Individuals with this form typically have ...
    https://medlineplus.gov/genetics/gene/col4a4 - Genetics
  6. Jackson-Weiss syndrome 
    ... feet. FGFR2 ... Agochukwu NB, Solomon BD, Muenke M. Hearing loss in syndromic craniosynostoses: otologic manifestations and clinical findings. ...
    https://medlineplus.gov/genetics/condition/jackson-weiss-syndrome - Genetics
  7. Bart-Pumphrey syndrome 
    ... impulses. GJB2 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ... Biochim Biophys Acta. 2013 Jan;1828(1):167-78. doi: 10.1016/j.bbamem.2012.06.024. Epub 2012 Jul 13. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/genetics/condition/bart-pumphrey-syndrome - Genetics
  8. Hystrix-like ichthyosis with deafness 
    ... not. GJB2 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ... Biochim Biophys Acta. 2013 Jan;1828(1):167-78. doi: 10.1016/j.bbamem.2012.06.024. Epub 2012 Jul 13. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/.../hystrix-like-ichthyosis-with-deafness - Genetics
  9. CHARGE syndrome 
    ... mutations in the CHD7 gene, it follows an autosomal dominant pattern of inheritance, which means one copy of ...
    https://medlineplus.gov/genetics/condition/charge-syndrome - Genetics
  10. Vohwinkel syndrome 
    ... GJB2 LORICRIN This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/vohwinkel-syndrome - Genetics
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