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Pfeiffer syndrome
acrocephalosyndactylia that has material basis in mutations in the FGFR1 and FGFR2 gene which results in premature fusion located in skull
Details
- Subclass of
- acrocephalosyndactylia, autosomal dominant disease
- different from
- infectious mononucleosis
- health specialty
- rheumatology
- ICPC 2 ID
- A90
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