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What is Van Allen Myhre syndrome?

What is Van Allen Myhre syndrome?

  • Van Allen Myhre syndrome: A syndrome which is characterised by vesicles, celosomia, short neck, microcornea, and dextrocardia.

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

Van Allen Myhre syndrome: Introduction

Types of Van Allen Myhre syndrome:

Broader types of Van Allen Myhre syndrome:

What causes Van Allen Myhre syndrome?

Causes of Van Allen Myhre syndrome: see causes of Van Allen Myhre syndrome

What are the symptoms of Van Allen Myhre syndrome?

Symptoms of Van Allen Myhre syndrome: see symptoms of Van Allen Myhre syndrome

Van Allen Myhre syndrome: Testing

Diagnostic testing: see tests for Van Allen Myhre syndrome.

Misdiagnosis: see misdiagnosis and Van Allen Myhre syndrome.

How is it treated?

Doctors and Medical Specialists for Van Allen Myhre syndrome: Neonatologist ; see also doctors and medical specialists for Van Allen Myhre syndrome.
Treatments for Van Allen Myhre syndrome: see treatments for Van Allen Myhre syndrome

Name and Aliases of Van Allen Myhre syndrome

Main name of condition: Van Allen Myhre syndrome

Other names or spellings for Van Allen Myhre syndrome:

Vesicles, celosomia, short neck, microcornea and dextrocardia

Van Allen Myhre syndrome: Related Conditions

Research the causes of these diseases that are similar to, or related to, Van Allen Myhre syndrome:

 

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