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Classical (Type I) Lissencephaly and Miller-Dieker Syndrome

✍ Scribed by Christine A. Matarese; Deborah L. Renaud


Book ID
116825488
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
126 KB
Volume
40
Category
Article
ISSN
0887-8994

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πŸ“œ SIMILAR VOLUMES


Prenatal diagnosis of lissencephaly: Mil
✍ John P. McGahan; Arthur Grix; Eugenio O. Gerscovich πŸ“‚ Article πŸ“… 1994 πŸ› John Wiley and Sons 🌐 English βš– 428 KB

Lissencephaly is a rare developmental disorder resulting from impaired neural migration occurring from 6 to 15 weeks' gestation.' In its most severe form, it results in complete absence of gyri and sulci, and is called agyria. In other cases, there may be only a few abnormal gyri. Prenatal diagnosis

Agyria β€” pachygyria and Miller-Dieker sy
✍ C. Dhellemmes; S. Girard; O. Dulac; O. Robain; A. Choiset; S. Tapia πŸ“‚ Article πŸ“… 1988 πŸ› Springer 🌐 English βš– 504 KB

Twelve cases of lissencephaly are reported. A high resolution chromosome study was performed on each in order to detect small chromosomal anomalies, undetectable with routine techniques. Only one case was shown to have an unbalanced karyotype with a microdeletion of the short arm of chromosome 17 (d