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Acromesomelic dysplasia Brahimi Bacha type

Acromesomelic dysplasia Brahimi Bacha type: Introduction

Acromesomelic dysplasia Brahimi Bacha type: A very rare genetic malformation syndrome characterized primarily by developmental abnormalities of the face and skeletal bones. More detailed information about the symptoms, causes, and treatments of Acromesomelic dysplasia Brahimi Bacha type is available below.

Symptoms of Acromesomelic dysplasia Brahimi Bacha type

Causes of Acromesomelic dysplasia Brahimi Bacha type

Read more about causes of Acromesomelic dysplasia Brahimi Bacha type.

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Definitions of Acromesomelic dysplasia Brahimi Bacha type:

Acromesomelic dysplasia Brahimi Bacha type is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Acromesomelic dysplasia Brahimi Bacha type, or a subtype of Acromesomelic dysplasia Brahimi Bacha type, 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 Acromesomelic dysplasia Brahimi Bacha type as a "rare disease".
Source - Orphanet

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More information about Acromesomelic dysplasia Brahimi Bacha type

  1. Acromesomelic dysplasia Brahimi Bacha type: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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