Say Meyer syndrome (medical condition): A very rare syndrome characterized mainly by short stature, developmental delay and trigonocephaly (premature fusion of skull bones giving the forehead a triangular shape).
See also:
Say-Meyer syndrome:
»Introduction: Say-Meyer syndrome
»Symptoms of Say-Meyer syndrome
Say Meyer syndrome: Trigonocephaly, short stature, and retarded psychomotor development.
Source: Diseases Database
These medical condition or symptom topics may be relevant to medical information for Say Meyer syndrome:
Say Meyer syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Say Meyer syndrome, or a subtype of Say Meyer 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 if affects 1 person per 2,000.
They list Say Meyer syndrome as a "rare disease".
Source - Orphanet
Say Meyer syndrome (medical condition): See Say-Meyer syndrome (disease information).
»Introduction: Say-Meyer syndrome
»Symptoms of Say-Meyer syndrome
Source - NIH
Source: Diseases Database
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