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What is Waardenburg syndrome type IIA?

What is Waardenburg syndrome type IIA?

  • Waardenburg syndrome type IIA: A rare genetic disorder characterized by partial albinism and have a greater hearing impairment than Waardenburg syndrome type I. Type 2A is distinguished from other forms of type 2 in the origin of the genetic defect - MITF gene on chromosome 3p14.1-p12.3.

Waardenburg syndrome type IIA: Introduction

Types of Waardenburg syndrome type IIA:

Broader types of Waardenburg syndrome type IIA:

What causes Waardenburg syndrome type IIA?

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

What are the symptoms of Waardenburg syndrome type IIA?

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

Can anyone else get Waardenburg syndrome type IIA?

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

Waardenburg syndrome type IIA: Testing

Diagnostic testing: see tests for Waardenburg syndrome type IIA.

Misdiagnosis: see misdiagnosis and Waardenburg syndrome type IIA.

How is it treated?

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

Name and Aliases of Waardenburg syndrome type IIA

Main name of condition: Waardenburg syndrome type IIA

Other names or spellings for Waardenburg syndrome type IIA:

Waardenburg syndrome type 2A

 

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