| Literature DB >> 33799212 |
Michela Bisciglia1, Roseline Froissart2, Anne Laure Bedat-Millet3, Norma Beatriz Romero4, Magali Pettazzoni5, Jean-Yves Hogrel6, François M Petit7, Tanya Stojkovic8.
Abstract
Muscle phosphorylase kinase b deficiency (PhK) is a rare disorder of glycogen metabolism characterized by exercise-induced myalgia and cramps, myoglobinuria and progressive muscle weakness. PhK deficiency is due to mutations in the PHKA1 gene inherited in an X-linked manner and is associated to glycogenosis type VIII (GSD VIII also called GSD IXd). PHKA1 gene codes for the αM subunit of the PhK, a multimeric protein complex responsible for the control of glycogen breakdown in muscle. Until now, few patients have been reported with X-linked recessive muscle PhK deficiency due to PHKA1 mutations. All reported patients presented with exercise intolerance and mild myopathy and one of them had cognitive impairment, leading to speculate about a central nervous system involvement in GSD VIII. Here we report in a sibling a novel mutation in the PHKA1 gene associated with a progressive myopathy, exercise intolerance, muscle hypertrophy and cognitive impairment as an associated feature. This report expands the genetic and clinical spectrum of the extremely rare PHKA1-related PhK deficiency and presents new evidences about its involvement in brain development.Entities:
Keywords: Cognitive impairment; Muscle glycogenosis; Myopathy; Phosphorylase b kinase
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Year: 2021 PMID: 33799212 DOI: 10.1016/j.jns.2021.117391
Source DB: PubMed Journal: J Neurol Sci ISSN: 0022-510X Impact factor: 3.181