Acromesomelic dysplasia, Maroteaux type: A rare genetic syndrome characterized by various developmental abnormalities of the skeletal bones and facial anomalies. More detailed information about the symptoms, causes, and treatments of Acromesomelic dysplasia, Maroteaux type is available below.
See full list of 17 symptoms of Acromesomelic dysplasia, Maroteaux type
Read more about causes of Acromesomelic dysplasia, Maroteaux type.
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Acromesomelic dysplasia, Maroteaux 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, Maroteaux type, or a subtype of Acromesomelic dysplasia, Maroteaux 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, Maroteaux type as a "rare disease".
Source - Orphanet
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