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Results 1 - 8 of 8 for Hearing "loss," autosomal dominant 83
  1. ... Kunst HP, Hoefsloot EH, Cruysberg JR, Cremers CW. Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1. Mol ...
  2. ... I, II, and III are inherited in an autosomal dominant pattern, which means one copy of the altered ... their family.Marshall syndrome also typically has an autosomal dominant pattern of inheritance.Stickler syndrome types IV, V, ...
  3. ... TCOF1 or POLR1D gene, it is considered an autosomal dominant condition, which means one copy of the altered ... the disorder in their family. In the remaining autosomal dominant cases, a person with Treacher Collins syndrome inherits ...
  4. Physical Therapy for Facioscapulohumeral Muscular Dystrophy (FSHD) (FacioScapuloHumeral Muscular Dystrophy Society) - PDF  
    Muscular Dystrophy/Living With ... Muscular Dystrophy ... FacioScapuloHumeral Muscular Dystrophy Society ... PDF
  5. ... the KMT2D gene, it is inherited in an autosomal dominant pattern, which means one copy of the altered ...
  6. ... conditions. SALL4 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
  7. ... Suomalainen A, Spelbrink JN. Twinkle mutations associated with autosomal dominant progressive external ophthalmoplegia lead to impaired helicase function ...
  8. Leukodystrophy From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Leukodystrophies/Start Here ... Leukodystrophies ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Leukodystrophy ...