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What is McGillivray syndrome?

What is McGillivray syndrome?

  • McGillivray syndrome: A very rare syndrome characterized mainly by heart defects, skull and facial abnormalities and ambiguous genitalia.

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

McGillivray syndrome: Introduction

Types of McGillivray syndrome:

Broader types of McGillivray syndrome:

What causes McGillivray syndrome?

Causes of McGillivray syndrome: see causes of McGillivray syndrome

What are the symptoms of McGillivray syndrome?

Symptoms of McGillivray syndrome: see symptoms of McGillivray syndrome

McGillivray syndrome: Testing

Diagnostic testing: see tests for McGillivray syndrome.

Misdiagnosis: see misdiagnosis and McGillivray syndrome.

How is it treated?

Doctors and Medical Specialists for McGillivray syndrome: Neonatologist, Cardiologist ; see also doctors and medical specialists for McGillivray syndrome.
Treatments for McGillivray syndrome: see treatments for McGillivray syndrome

Name of McGillivray syndrome

Main name of condition: McGillivray syndrome


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