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Pfeiffer syndrome: Systemic and ocular implications

✍ Scribed by Elise Harb; Barry Kran


Book ID
119337547
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
264 KB
Volume
76
Category
Article
ISSN
1529-1839

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πŸ“œ SIMILAR VOLUMES


Pfeiffer syndrome
✍ Winter, Robin M. πŸ“‚ Article πŸ“… 1994 πŸ› John Wiley and Sons 🌐 English βš– 47 KB
Favorable prognosis for children with Pf
✍ Robin, Nathaniel H.; Scott, Jennifer A.; Arnold, James E.; Goldstein, Jeffrey A. πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 36 KB πŸ‘ 2 views

Pfeiffer syndrome (PS) is an autosomal dominant condition comprising bilateral coronal craniosynostosis, midface hypoplasia with a beaked nasal tip, and broad and medially deviated thumbs and great toes. It is a clinically variable disorder and has been divided into three subtypes [Cohen, 1993: Am J