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Usher syndrome, type IIIA

Usher syndrome, type IIIA: Introduction

Usher syndrome, type IIIA: A rare inherited disorder where children are born with normal hearing and vision which progressively deteriorates at a variable rate. The defect occurs on chromosome 5q14. More detailed information about the symptoms, causes, and treatments of Usher syndrome, type IIIA is available below.

Symptoms of Usher syndrome, type IIIA

  • Hearing loss #onset by teenage years
  • Deafness #by late adulthood
  • Night blindness #onset during puberty
  • Blindness #by mid-adulthood
  • Progressive balance impairment
  • more symptoms...»

Home Diagnostic Testing

Home medical testing related to Usher syndrome, type IIIA:

Wrongly Diagnosed with Usher syndrome, type IIIA?

Causes of Usher syndrome, type IIIA

Read more about causes of Usher syndrome, type IIIA.

Usher syndrome, type IIIA: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Usher syndrome, type IIIA

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as multiple sclerosis (see more »

Usher syndrome, type IIIA: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Usher syndrome, type IIIA: Animations

Prognosis for Usher syndrome, type IIIA

Prognosis for Usher syndrome, type IIIA: hearing and vision loss starts during the first few decades of life with deafness usually by middle age

Usher syndrome, type IIIA: Broader Related Topics

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Related Usher syndrome, type IIIA Info

More information about Usher syndrome, type IIIA

  1. Usher syndrome, type IIIA: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Prognosis

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