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Epilepsy in KBG Syndrome: Report of Additional Cases.

Pediatric neurology - 1 Feb 2024

Whitney Robyn, Komar Madeline, Yoganathan Sangeetha, Costain Gregory, Jain Puneet

Abstract excerpt

BACKGROUND: KBG syndrome is a genetic disorder characterized by short stature, dysmorphic features, macrodontia, cognitive impairment, and limb anomalies. Epilepsy is an important comorbidity associated with KBG syndrome, although the entire phenotypic spectrum may not be fully appreciated. METHODS: We identified five new patients with KBG syndrome-related epilepsy and compared their phenotype to previously...

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Identifiers

PMID: 38157719
DOI: 10.1016/j.pediatrneurol.2023.12.006

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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