3-M Syndrome: A rare genetic condition which is characterized by distinctive physical features and severe growth retardation that starts during the fetal stage. Intelligence is not affected. More detailed information about the symptoms, causes, and treatments of 3-M Syndrome is available below.
See full list of 26 symptoms of 3-M Syndrome
Read more about complications of 3-M Syndrome.
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3-M Syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that 3-M Syndrome, or a subtype of 3-M Syndrome,
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 3-M Syndrome as a "rare disease".
Source - Orphanet
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