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Somatic mosaicism for PDHA1 mutation in a male with pyruvate dehydrogenase complex deficiency
Curtis R Coughlin1, Ian D Krantz, Eric S Schmitt
1Section of Metabolic Disease, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Abstract:
Pyruvate dehydrogenase complex deficiency is a clinically heterogeneous disorder. Most cases are due to mutations in an X-linked PDHA1 gene encoding the E1alpha subunit of the multienzyme complex. Females with mutations in the PDHA1 gene may be asymptomatic or have a milder phenotype as a result of skewed X-inactivation, while males are typically more severely affected. We report a case of PDHA1 mosaicism in a male patient who had a milder phenotype.
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