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Pfeiffer type acrocephalosyndactyly (medical condition): A rare genetic disorder where some of the skull bones fuse too early which...more »
See also:
Pfeiffer syndrome:
»Introduction: Pfeiffer syndrome
»Symptoms of Pfeiffer syndrome
These medical condition or symptom topics may be relevant to medical information for Pfeiffer type acrocephalosyndactyly:
Pfeiffer type acrocephalosyndactyly is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Pfeiffer type acrocephalosyndactyly, or a subtype of Pfeiffer type acrocephalosyndactyly,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Pfeiffer type acrocephalosyndactyly: Another name for Pfeiffer syndrome (or close medical condition association).
»Introduction: Pfeiffer syndrome
»Symptoms of Pfeiffer syndrome
Pfeiffer type acrocephalosyndactyly: Pfeiffer type acrocephalosyndactyly is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of Pfeiffer type acrocephalosyndactyly incude:
See full list of 16 symptoms of Pfeiffer type acrocephalosyndactyly (Pfeiffer syndrome)
These medical disease topics may be related to Pfeiffer type acrocephalosyndactyly:
Source - NIH
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