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Mende syndrome

Mende syndrome: Introduction

Mende syndrome: A rare condition characterized by congenital deafness, mutism, partial albinism and a mongoloid face as well as other anomalies. More detailed information about the symptoms, causes, and treatments of Mende syndrome is available below.

Symptoms of Mende syndrome

Home Diagnostic Testing

Home medical testing related to Mende syndrome:

Wrongly Diagnosed with Mende syndrome?

Causes of Mende syndrome

Read more about causes of Mende syndrome.

Disease Topics Related To Mende syndrome

Research the causes of these diseases that are similar to, or related to, Mende syndrome:

Less Common Symptoms of Mende syndrome

Misdiagnosis and Mende syndrome

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Mende syndrome: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Mende syndrome: Animations

Statistics for Mende syndrome

Mende syndrome: Broader Related Topics

User Interactive Forums

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Definitions of Mende syndrome:

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

Related Mende syndrome Info

More information about Mende syndrome

  1. Mende syndrome: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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