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Deafness, autosomal dominant nonsyndromic sensorineural 41

Deafness, autosomal dominant nonsyndromic sensorineural 41: Introduction

Deafness, autosomal dominant nonsyndromic sensorineural 41: Dominantly inherited hearing loss that occurs without any other symptoms - i.e. is not associated with any other condition. Type 41 involves a defect on chromosome 12q24.32-qter. More detailed information about the symptoms, causes, and treatments of Deafness, autosomal dominant nonsyndromic sensorineural 41 is available below.

Symptoms of Deafness, autosomal dominant nonsyndromic sensorineural 41

Treatments for Deafness, autosomal dominant nonsyndromic sensorineural 41

  • Management of sensorineural deafness depends upon the degree of hearing loss, the type of hearing loss, the age of the patient at the time of diagnosis, and patient preference. Conductive hearing loss may coexist, and remediable causes should be sought. Treatments include:
    • Education for patients, families and carers
    • Treatment of remediable causes
      • Ear wax removal
      • Surgery for acoustic neuroma or cholesteatoma
  • more treatments...»

Home Diagnostic Testing

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Wrongly Diagnosed with Deafness, autosomal dominant nonsyndromic sensorineural 41?

Causes of Deafness, autosomal dominant nonsyndromic sensorineural 41

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Deafness, autosomal dominant nonsyndromic sensorineural 41: Undiagnosed Conditions

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Deafness, autosomal dominant nonsyndromic sensorineural 41: Rare Types

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More information about Deafness, autosomal dominant nonsyndromic sensorineural 41

  1. Deafness, autosomal dominant nonsyndromic sensorineural 41: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Types
 

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