𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A new syndrome with camptodactyly, joint contractures, facial anomalies, and skeletal defects: a case report and review of syndromes with camptodactyly

✍ Scribed by M. M. Rozin; M. Hertz; R. M. Goodman


Book ID
119839607
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
826 KB
Volume
26
Category
Article
ISSN
0009-9163

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


The Pointer syndrome: A new syndrome wit
✍ Huq, A.H.M. Mahbubul; Braverman, Richard M.; Greenberg, Frank; Bacino, Carlos A. πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 423 KB πŸ‘ 1 views

We describe a brother and sister with a unique combination of skeletal findings including camptodactyly (phalangeal dislocations), facial anomalies, neonatal respiratory problems, and feeding problems due to poor suck. Metaphyseal splaying, osteopenia, endosteal bone apposition, campomelia, and mult

The Tel Hashomer camptodactyly syndrome:
✍ Pagnan, Nina Amalia Brancia ;Gollop, Thomaz Rafael ;Lederman, Henrique ;Optiz, J πŸ“‚ Article πŸ“… 1988 πŸ› John Wiley and Sons 🌐 English βš– 347 KB πŸ‘ 3 views

We report on a new case of Tel Hashomer camptodactyly syndrome and review the literature. This syndrome is characterized by skeletal dysplasia, muscle hypoplasia, camptodactyly, and abnormal dermatoglyphics. The inheritance is autosomal recessive with probable partial expression in the heterozygote.