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Usher syndrome, type 1F

Usher syndrome, type 1F: Introduction

Usher syndrome, type 1F: 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 10q21-q22. More detailed information about the symptoms, causes, and treatments of Usher syndrome, type 1F is available below.

Symptoms of Usher syndrome, type 1F

Home Diagnostic Testing

Home medical testing related to Usher syndrome, type 1F:

Wrongly Diagnosed with Usher syndrome, type 1F?

Causes of Usher syndrome, type 1F

Read more about causes of Usher syndrome, type 1F.

Disease Topics Related To Usher syndrome, type 1F

Research the causes of these diseases that are similar to, or related to, Usher syndrome, type 1F:

Usher syndrome, type 1F: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Usher syndrome, type 1F

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 more »

Usher syndrome, type 1F: Research Doctors & Specialists

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Other doctor, physician and specialist research services:

Usher syndrome, type 1F: Animations

Usher syndrome, type 1F: Broader Related Topics

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Related Usher syndrome, type 1F Info

More information about Usher syndrome, type 1F

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

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