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Article

Callosal alterations in pyridoxine-dependent epilepsy.

Developmental medicine and child neurology - 1 Nov 2014

Friedman Seth D, Ishak Gisele E, Poliachik Sandra L, Poliakov Andrew V, Otto Randolph K, Shaw Dennis W W, Willemsen Michèl A, Bok Levinus A, Gospe Sidney M

Abstract excerpt

AIM: While there have been isolated reports of callosal morphology differences in pyridoxine-dependent epilepsy (PDE), a rare autosomal disorder caused by ALDH7A1 gene mutations, no study has systematically evaluated callosal features in a large sample of patients. This study sought to overcome this knowledge gap. METHOD: Spanning a wide age range from birth to 48 years, corpus callosum morphology and...

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Identifiers

PMID: 24942048
DOI: 10.1111/dmcn.12511

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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