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What is Morava-Mehes syndrome?

What is Morava-Mehes syndrome?

  • Morava-Mehes syndrome: A rare syndrome characterized mainly by an underdeveloped bones in the forearm, calf and fourth and fifth fingers, short stature and unusual facial appearance.

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

Morava-Mehes syndrome: Introduction

Types of Morava-Mehes syndrome:

Broader types of Morava-Mehes syndrome:

What causes Morava-Mehes syndrome?

Causes of Morava-Mehes syndrome: see causes of Morava-Mehes syndrome

What are the symptoms of Morava-Mehes syndrome?

Symptoms of Morava-Mehes syndrome: see symptoms of Morava-Mehes syndrome

Morava-Mehes syndrome: Testing

Diagnostic testing: see tests for Morava-Mehes syndrome.

Misdiagnosis: see misdiagnosis and Morava-Mehes syndrome.

How is it treated?

Doctors and Medical Specialists for Morava-Mehes syndrome: Orthopedic Surgeon ; see also doctors and medical specialists for Morava-Mehes syndrome.
Treatments for Morava-Mehes syndrome: see treatments for Morava-Mehes syndrome

Name and Aliases of Morava-Mehes syndrome

Main name of condition: Morava-Mehes syndrome

Other names or spellings for Morava-Mehes syndrome:

Ulnar/fibula ray defect [brachydactyly]

 

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