๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Prevalence of Angelman syndrome amongst referrals with epilepsy and developmental delay

โœ Scribed by Angela F. Davies; Caroline Mackie Ogilvie


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
74 KB
Volume
143A
Category
Article
ISSN
1552-4825

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Adamsโ€“Oliver syndrome in siblings with c
โœ Robin R. McGoey; Yves Lacassie ๐Ÿ“‚ Article ๐Ÿ“… 2008 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 316 KB ๐Ÿ‘ 1 views

## Abstract Adamsโ€“Oliver syndrome (AOS) is a wellโ€known rare syndrome of cutis aplasia in combination with limb defects. Recent reports have been published discussing the clinical variability and apparent genetic heterogeneity seen in some affected individuals and families with particular attention

Albinism and agenesis of the corpus call
โœ del Campo, Miguel; Hall, Bryan D.; Aeby, Alec; Nassogne, Marie-Cecile; Verloes, ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 38 KB ๐Ÿ‘ 2 views

We report on two sibs and two other unrelated patients with agenesis of corpus callosum, oculocutaneous albinism, repeated infections, and cardiomyopathy. All manifested postnatal growth retardation, microcephaly, and profound developmental delay. Additional central nervous system anomalies present