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Usher Syndrome 1H

Usher Syndrome 1H: Introduction

Usher Syndrome 1H: A rare inherited disorder characterized by sensorineural deafness and progressive vision loss which starts during the first decade of life and blindness usually occurs between 20-35 years of age. Symptoms are generally more severe than in type 2 with deafness occurring at birth or during first year and vision loss starting during childhood. The defect occurs on chromosome 17q24-q25. More detailed information about the symptoms, causes, and treatments of Usher Syndrome 1H is available below.

Symptoms of Usher Syndrome 1H

Home Diagnostic Testing

Home medical testing related to Usher Syndrome 1H:

Wrongly Diagnosed with Usher Syndrome 1H?

Causes of Usher Syndrome 1H

Read more about causes of Usher Syndrome 1H.

Usher Syndrome 1H: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Usher Syndrome 1H

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

Usher Syndrome 1H: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Usher Syndrome 1H: Animations

Usher Syndrome 1H: Broader Related Topics

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Related Usher Syndrome 1H Info

More information about Usher Syndrome 1H

  1. Usher Syndrome 1H: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing

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