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What is Waardenburg syndrome type IIE?

What is Waardenburg syndrome type IIE?

  • Waardenburg syndrome type IIE: A rare genetic disorder characterized by partial albinism and have a greater hearing impairment than Waardenburg syndrome type I. Type 2E is distinguished from other forms of type 2 in the origin of the genetic defect - SOX10 gene on chromosome 22q13.

Waardenburg syndrome type IIE: Introduction

Types of Waardenburg syndrome type IIE:

Broader types of Waardenburg syndrome type IIE:

What causes Waardenburg syndrome type IIE?

Causes of Waardenburg syndrome type IIE: see causes of Waardenburg syndrome type IIE

What are the symptoms of Waardenburg syndrome type IIE?

Symptoms of Waardenburg syndrome type IIE: see symptoms of Waardenburg syndrome type IIE

Can anyone else get Waardenburg syndrome type IIE?

More information: see contagiousness of Waardenburg syndrome type IIE
Inheritance: see inheritance of Waardenburg syndrome type IIE

Waardenburg syndrome type IIE: Testing

Diagnostic testing: see tests for Waardenburg syndrome type IIE.

Misdiagnosis: see misdiagnosis and Waardenburg syndrome type IIE.

How is it treated?

Doctors and Medical Specialists for Waardenburg syndrome type IIE: Medical Geneticist ; see also doctors and medical specialists for Waardenburg syndrome type IIE.
Treatments for Waardenburg syndrome type IIE: see treatments for Waardenburg syndrome type IIE

Name and Aliases of Waardenburg syndrome type IIE

Main name of condition: Waardenburg syndrome type IIE

Other names or spellings for Waardenburg syndrome type IIE:

Waardenburg syndrome type 2E

 

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