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Results 1 - 10 of 12 for Hereditary hearing loss deafness
  1. Nonsyndromic hearing loss 
    ... Testing Registry: X-linked deafness Genetic Testing Registry: Hereditary hearing loss and deafness Nonsyndromic hereditary sensorineural hearing loss National Organization for ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  2. Palmoplantar keratoderma with deafness 
    ... S. The GJB2 mutation R75Q can cause nonsyndromic hearing loss DFNA3 or hereditary palmoplantar keratoderma with deafness. Am J Med Genet A. 2005 Aug 30; ...
    https://medlineplus.gov/.../palmoplantar-keratoderma-with-deafness - Genetics
  3. Hereditary sensory and autonomic neuropathy type IE 
    ... their family. DNMT1-complex disorder DNMT1-related dementia, deafness, and sensory neuropathy Hereditary sensory and autonomic neuropathy type 1 with dementia and hearing loss Hereditary sensory neuropathy type IE HSAN1E HSN IE ...
    https://medlineplus.gov/...-sensory-and-autonomic-neuropathy-type-ie - Genetics
  4. MT-TS1 gene 
    ... Citation on PubMed Usami SI, Nishio SY. Nonsyndromic Hearing Loss and Deafness, Mitochondrial. 2004 Oct 22 [updated 2018 Jun 14]. ...
    https://medlineplus.gov/genetics/gene/mt-ts1 - Genetics
  5. Familial cold autoinflammatory syndrome type 2 
    ... diarrhea, headache, and nausea. Some affected individuals develop hearing loss (sensorineural deafness) due to chronic inflammation. Familial cold autoinflammatory syndrome ...
    https://medlineplus.gov/...ial-cold-autoinflammatory-syndrome-type-2 - Genetics
  6. Charcot-Marie-Tooth disease 
    ... affected individuals have loss of vision or gradual hearing loss that sometimes leads to deafness.There are several types of Charcot-Marie-Tooth ... WITH EXCESSIVE MYELIN FOLDING COMPLEX, AUTOSOMAL RECESSIVE NEUROPATHY, ... IMPAIRED INTELLECTUAL DEVELOPMENT, AND ABSENT SENSORY LARGE MYELINATED ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  7. DNMT1 gene 
    ... Smith DI, Dyck PJ. Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss. Nat Genet. 2011 Jun;43(6):595-600. ...
    https://medlineplus.gov/genetics/gene/dnmt1 - Genetics
  8. Alport syndrome 
    ... have only hematuria (thin basement membrane nephropathy). Congenital hereditary hematuria Hematuria-nephropathy-deafness syndrome Hematuric hereditary nephritis Hemorrhagic familial nephritis Hemorrhagic ...
    https://medlineplus.gov/genetics/condition/alport-syndrome - Genetics
  9. Autosomal dominant optic atrophy and cataract 
    ... shaking (tremors). In some cases, affected individuals have hearing loss caused by abnormalities of the inner ear (sensorineural deafness). Autosomal dominant optic atrophy and cataract is one ...
    https://medlineplus.gov/...somal-dominant-optic-atrophy-and-cataract - Genetics
  10. Mitochondrial DNA 
    ... and MT-TE, can cause mitochondrial diabetes and deafness (MIDD). People with this condition have diabetes and sometimes hearing loss, particularly of high tones. The MT-TL1, MT- ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics
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