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Transient global amnesia associated with an acute infarction in the retrosplenium of the corpus callosum

✍ Scribed by Kozue Saito; Kazumi Kimura; Kazuo Minematsu; Atsushi Shiraishi; Makoto Nakajima

Book ID
119465942
Publisher
Elsevier Science
Year
2003
Tongue
English
Weight
110 KB
Volume
210
Category
Article
ISSN
0022-510X

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Patient with an Xp21 contiguous gene del
Patient with an Xp21 contiguous gene deletion syndrome in association with agenesis of the corpus callosum
✍ Baranzini, Sergio E.; del Rey, Graciela; Nigro, Nora; Szijan, Irene; Chamoles, N πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 761 KB

The so-called Xp21 contiguous deletion syndrome or complex glycerol kinase deficiency (GKD) usually presents with classical Duchenne muscular dystrophy (DMD) or a milder dystrophic myopathy, adrenal hypoplasia, and GKD. A number of syndromic and nonsyndromic cases of agenesis of the corpus callosum