Article
Pfeiffer syndrome.
Orphanet journal of rare diseases - 1 Jun 2006
Vogels Annick, Fryns Jean-Pierre
Abstract excerpt
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 slow development. Based on the severity of the phenotype, Pfeiffer syndrome is divided into three clinical subtypes....
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
