𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Coffin-Lowry syndrome: A 20-year follow-up and review of long-term outcomes

✍ Scribed by Hunter, Alasdair G.W.

Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
327 KB
Volume
111
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Long-term follow-up of a 26-year-old mal
Long-term follow-up of a 26-year-old male with duplication of 16p: Clinical report and review
✍ Mascha K. Rochat; Mariluce Riegel; Albert A. Schinzel πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 308 KB πŸ‘ 1 views

## Abstract We report on a 26‐year‐old male with profound psychomotor retardation and a pattern of dysmorphic features and malformations characteristic for duplication of the short arm of chromosome 16. He has an elongated face, sparse hair, upslanting palpebral fissures, anteverted nostrils, hypop

Zimmermann-Laband syndrome in an adult.
Zimmermann-Laband syndrome in an adult. Long-term follow-up of a patient with vascular and cardiac complications
✍ Robertson, Stephen P.; Lipp, Harry; Bankier, Agnes πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 37 KB πŸ‘ 2 views

Zimmermann-Laband syndrome (ZLS) is characterised by findings of coarse facial appearance, hepatosplenomegaly, and hirsutism often first observed in infancy, followed by the evolution during childhood of gingival fibromatosis, small joint hyperextensibility, and hypoplasia of the finger-and toenails