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Case study: A patient with agenesis of the corpus callosum with minimal associated neuropsychological impairment

✍ Scribed by Brescian, Natalie E.; Curiel, Rosie E.; Gass, Carlton S.

Book ID
120853376
Publisher
Taylor and Francis Group
Year
2013
Tongue
English
Weight
261 KB
Volume
20
Category
Article
ISSN
1355-4794

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πŸ“œ SIMILAR VOLUMES

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