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What is Microcephaly, autosomal dominant?

What is Microcephaly, autosomal dominant?

  • Microcephaly, autosomal dominant: A very rare inherited disorder characterized mainly by a small head, short stature and other anomalies.

Microcephaly, autosomal dominant is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Microcephaly, autosomal dominant, or a subtype of Microcephaly, autosomal dominant, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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

Microcephaly, autosomal dominant: Introduction

Types of Microcephaly, autosomal dominant:

Broader types of Microcephaly, autosomal dominant:

What causes Microcephaly, autosomal dominant?

Causes of Microcephaly, autosomal dominant: see causes of Microcephaly, autosomal dominant

What are the symptoms of Microcephaly, autosomal dominant?

Symptoms of Microcephaly, autosomal dominant: see symptoms of Microcephaly, autosomal dominant

Microcephaly, autosomal dominant: Testing

Diagnostic testing: see tests for Microcephaly, autosomal dominant.

Misdiagnosis: see misdiagnosis and Microcephaly, autosomal dominant.

How is it treated?

Doctors and Medical Specialists for Microcephaly, autosomal dominant: Medical Geneticist ; see also doctors and medical specialists for Microcephaly, autosomal dominant.
Treatments for Microcephaly, autosomal dominant: see treatments for Microcephaly, autosomal dominant

Name and Aliases of Microcephaly, autosomal dominant

Main name of condition: Microcephaly, autosomal dominant

Other names or spellings for Microcephaly, autosomal dominant:

Microcephaly with autosomal dominant inheritance

Microcephaly with autosomal dominant inheritance
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

 

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