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Deafness, autosomal dominant nonsyndromic sensorineural 21

Deafness, autosomal dominant nonsyndromic sensorineural 21: Introduction

Deafness, autosomal dominant nonsyndromic sensorineural 21: Dominantly inherited hearing loss that occurs without any other symptoms - i.e. is not associated with any other condition. Type 21 involves a defect on chromosome 6p21.3. More detailed information about the symptoms, causes, and treatments of Deafness, autosomal dominant nonsyndromic sensorineural 21 is available below.

Symptoms of Deafness, autosomal dominant nonsyndromic sensorineural 21

Treatments for Deafness, autosomal dominant nonsyndromic sensorineural 21

  • Treatment 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 21?

Causes of Deafness, autosomal dominant nonsyndromic sensorineural 21

Read more about causes of Deafness, autosomal dominant nonsyndromic sensorineural 21.

Deafness, autosomal dominant nonsyndromic sensorineural 21: Undiagnosed Conditions

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Misdiagnosis and Deafness, autosomal dominant nonsyndromic sensorineural 21

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Deafness, autosomal dominant nonsyndromic sensorineural 21: Research Doctors & Specialists

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Deafness, autosomal dominant nonsyndromic sensorineural 21: Rare Types

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Deafness, autosomal dominant nonsyndromic sensorineural 21: Animations

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More information about Deafness, autosomal dominant nonsyndromic sensorineural 21

  1. Deafness, autosomal dominant nonsyndromic sensorineural 21: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Types
 

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