𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Vohwinkel syndrome (mutilating keratoderma) associated with craniofacial anomalies

✍ Scribed by Sensi, A. ;Bettoli, V. ;Zampino, M. R. ;Gandini, E. ;Calzolari, E.


Publisher
John Wiley and Sons
Year
1994
Tongue
English
Weight
250 KB
Volume
50
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


A new skeletal dysplasia syndrome with d
✍ Jones, Kenneth Lee ;Jones, Kenneth Lyons ;Miller, Kenneth ;Opitz, John M. ;Reyno πŸ“‚ Article πŸ“… 1986 πŸ› John Wiley and Sons 🌐 English βš– 360 KB πŸ‘ 1 views

We report on a boy from a consanguinous marriage who has a unique skeletal dysplasia, marked dwarfism, mild developmental delay, eye abnormalities, and cranofacial and skeletal changes that have not been described previously.

Severe form of Freeman-Sheldon syndrome
✍ Zampino, Giuseppe; Conti, Guido; Balducci, Francesca; Moschini, Massimo; Macchia πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 17 KB πŸ‘ 1 views

We describe a child with whistling face and multiple contractures, including ulnar deviation of fingers, compatible with a diagnosis of Freeman-Sheldon syndrome (FSS). This patient also presented severe hypertonicity, multiple episodes of pneumonia, difficulty in swallowing, and poor weight gain, wh