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Usher syndrome, type IIIB

Usher syndrome, type IIIB: Introduction

Usher syndrome, type IIIB: 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 20q. More detailed information about the symptoms, causes, and treatments of Usher syndrome, type IIIB is available below.

Symptoms of Usher syndrome, type IIIB

  • 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 IIIB:

Wrongly Diagnosed with Usher syndrome, type IIIB?

Causes of Usher syndrome, type IIIB

Read more about causes of Usher syndrome, type IIIB.

Usher syndrome, type IIIB: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Usher syndrome, type IIIB

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as ...read more »

Usher syndrome, type IIIB: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Usher syndrome, type IIIB: Animations

Prognosis for Usher syndrome, type IIIB

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

Usher syndrome, type IIIB: Broader Related Topics

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Related Usher syndrome, type IIIB Info

More information about Usher syndrome, type IIIB

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

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