𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Central nervous system malformations in the CHARGE association

✍ Scribed by Lin, Angela E. ;Siebert, Joseph R. ;Graham, John M.


Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
715 KB
Volume
37
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.

✦ Synopsis


Of 144 patients with the CHARGE association (literature 136, new patients 8), 47 (33%) had either a postmortem examination (30) or computerized axial tomography scan (17) of the head. Twenty-six of 47 (55%) had definite central nervous system (CNS) malformations: arhinencephaly, with or without other defects (111, holoprosencephaly (21, holoprosencephaly with arhinencephaly (l), other forebrain defects (3), hindbrain defects (31, or other defects (6). The presence of CNS malformation was most strongly associated with choanal atresia. This review demonstrates a predominance of forebrain anomalies, particularly arhinencephaly and holoprosencephaly, which may provide a clue to the mechanism of abnormal morphogenesis involved in CHARGE association.


πŸ“œ SIMILAR VOLUMES


Central nervous system malformations in
✍ Nowaczyk, M.J.M.; Blaser, S.I.; Clarke, J.T.R. πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 35 KB πŸ‘ 2 views

Central nervous system malformations have been reported in a number of inherited enzyme defects. Ethylmalonic encephalopathy, an organic aciduria of unknown pathogenesis, has not been reported previously in association with brain or spinal cord malformations. We report on 2 sibs with confirmed ethyl

Zoonotic Ljungan virus associated with c
✍ Bo Niklasson; Annika Samsioe; Nikos Papadogiannakis; Susanne Gustafsson; William πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 136 KB

## Abstract ## BACKGROUND: The Ljungan virus (LV) has been shown to cause central nervous system malformations in laboratory mouse models. The LV has also been associated with intrauterine fetal death in humans. We investigated the presence of LV in a series of human hydrocephaly and anencephaly c