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Pfeiffer syndrome

Pfeiffer syndrome is a rare autosomal dominantly inherited disorder that associates craniosynostosis, broad and deviated thumbs and big toes, and partial syndactyly on hands and feet. Hydrocephaly may be found occasionally, along with severe ocular proptosis, ankylosed elbows, abnormal viscera, and...

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Bibliografske podrobnosti
Main Authors: Vogels, Annick, Fryns, Jean-Pierre
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2006
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1482682/
https://ncbi.nlm.nih.gov/pubmed/16740155
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-1-19
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