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What is Myhre-Ruvalcaba-Kelley syndrome?

What is Myhre-Ruvalcaba-Kelley syndrome?

  • Myhre-Ruvalcaba-Kelley syndrome: A rare recessively inherited X-linked disorder characterized by hearing impairment from birth and hypogonadism.

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Myhre-Ruvalcaba-Kelley syndrome as a "rare disease".
Source - Orphanet

Myhre-Ruvalcaba-Kelley syndrome: Introduction

Types of Myhre-Ruvalcaba-Kelley syndrome:

Broader types of Myhre-Ruvalcaba-Kelley syndrome:

What causes Myhre-Ruvalcaba-Kelley syndrome?

Causes of Myhre-Ruvalcaba-Kelley syndrome: see causes of Myhre-Ruvalcaba-Kelley syndrome

What are the symptoms of Myhre-Ruvalcaba-Kelley syndrome?

Symptoms of Myhre-Ruvalcaba-Kelley syndrome: see symptoms of Myhre-Ruvalcaba-Kelley syndrome

Myhre-Ruvalcaba-Kelley syndrome: Testing

Diagnostic testing: see tests for Myhre-Ruvalcaba-Kelley syndrome.

Misdiagnosis: see misdiagnosis and Myhre-Ruvalcaba-Kelley syndrome.

How is it treated?

Doctors and Medical Specialists for Myhre-Ruvalcaba-Kelley syndrome: Medical Geneticist ; see also doctors and medical specialists for Myhre-Ruvalcaba-Kelley syndrome.
Treatments for Myhre-Ruvalcaba-Kelley syndrome: see treatments for Myhre-Ruvalcaba-Kelley syndrome

Name and Aliases of Myhre-Ruvalcaba-Kelley syndrome

Main name of condition: Myhre-Ruvalcaba-Kelley syndrome

Other names or spellings for Myhre-Ruvalcaba-Kelley syndrome:

congenital deafness and hypogonadism

 

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