Mitochondrial HMG‐CoA Synthase Deficiency Presenting as Pediatric Metabolic Stroke: A Case Report of a Novel Homozygous HMGCS2 (p.Ile56Asn) Variant. - Alshami, Yasmeen; Hroub, Osama; Hroub, Mohammad; Abouodeh, Saja; Makhamre, Zahra; Hammouri, Ahmad G.; Alzatari, Ibrahim; Atawneh, Osama (Clinical Case Reports, 2025)