Deafness- autosomal dominant nonsyndromic sensorineural 3
Overview
Dominantly inherited hearing loss that occurs without any other symptoms - i.e. is not associated with any other condition. Type 3 involves a defect in the connexin-26 gene on chromosome 13q11-q12.
Symptoms
Sensorineural deafness
Diagnosis
This medical information about signs and symptoms for Deafness, autosomal dominant nonsyndromic sensorineural 3 has been gathered from various sources, may not be fully accurate, and may not be the full list of Deafness, autosomal dominant nonsyndromic sensorineural 3 signs or Deafness, autosomal dominant nonsyndromic sensorineural 3 symptoms. Furthermore, signs and symptoms of Deafness, autosomal dominant nonsyndromic sensorineural 3 may vary on an individual basis for each patient. Only your doctor can provide adequate diagnosis of any signs or symptoms and whether they are indeed Deafness, autosomal dominant nonsyndromic sensorineural 3 symptoms.