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Usher syndrome, type 1B

Usher syndrome, type 1B: Introduction

Usher syndrome, type 1B: A syndrome which is characterised by congenital bilateral sensorineural hearing loss. More detailed information about the symptoms, causes, and treatments of Usher syndrome, type 1B is available below.

Symptoms of Usher syndrome, type 1B

Home Diagnostic Testing

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

Wrongly Diagnosed with Usher syndrome, type 1B?

Usher syndrome, type 1B: Related Patient Stories

Causes of Usher syndrome, type 1B

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

Disease Topics Related To Usher syndrome, type 1B

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

Usher syndrome, type 1B: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Usher syndrome, type 1B

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...read more »

Usher syndrome, type 1B: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Usher syndrome, type 1B: Animations

Statistics for Usher syndrome, type 1B

Usher syndrome, type 1B: Broader Related Topics

User Interactive Forums

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Definitions of Usher syndrome, type 1B:

Usher syndrome, type 1B 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 1B, or a subtype of Usher syndrome, type 1B, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

 

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