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What is Myhre-Ruvalcaba-Graham syndrome?

What is Myhre-Ruvalcaba-Graham syndrome?

  • Myhre-Ruvalcaba-Graham syndrome: A rare disorder characterized by mental retardation, retarded growth before and after birth, early-onset deafness and facial anomalies as well as other problems.

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

Myhre-Ruvalcaba-Graham syndrome: Introduction

Types of Myhre-Ruvalcaba-Graham syndrome:

Broader types of Myhre-Ruvalcaba-Graham syndrome:

What causes Myhre-Ruvalcaba-Graham syndrome?

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

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

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

Myhre-Ruvalcaba-Graham syndrome: Testing

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

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

How is it treated?

Doctors and Medical Specialists for Myhre-Ruvalcaba-Graham syndrome: Neonatologist, Pediatrician ; see also doctors and medical specialists for Myhre-Ruvalcaba-Graham syndrome.
Treatments for Myhre-Ruvalcaba-Graham syndrome: see treatments for Myhre-Ruvalcaba-Graham syndrome

Name of Myhre-Ruvalcaba-Graham syndrome

Main name of condition: Myhre-Ruvalcaba-Graham syndrome


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