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Usher syndrome, type 1C

Usher syndrome, type 1C: Introduction

Usher syndrome, type 1C: 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 11p15.1. More detailed information about the symptoms, causes, and treatments of Usher syndrome, type 1C is available below.

Symptoms of Usher syndrome, type 1C

Home Diagnostic Testing

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

Wrongly Diagnosed with Usher syndrome, type 1C?

Usher syndrome, type 1C: Related Patient Stories

Causes of Usher syndrome, type 1C

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

Disease Topics Related To Usher syndrome, type 1C

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

Usher syndrome, type 1C: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Usher syndrome, type 1C

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Usher syndrome, type 1C: Research Doctors & Specialists

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Usher syndrome, type 1C: Animations

Statistics for Usher syndrome, type 1C

Usher syndrome, type 1C: Broader Related Topics

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Definitions of Usher syndrome, type 1C:

Usher syndrome, type 1C is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Usher syndrome, type 1C, or a subtype of Usher syndrome, type 1C, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)


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