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Neuromuscul Disord ; 31(5): 462-465, 2021 05.
Artigo em Inglês | MEDLINE | ID: mdl-33741226

RESUMO

Duchenne muscular dystrophy is an X-Linked neuromuscular disorder, and the most common muscular dystrophy. Neuropsychiatric phenotype associated to DMD gene mutations include now low IQ scores, epilepsy, autism, and attention deficit disorder. These have been observed with higher frequency in mutations that disrupt the short isoforms Dp71 and Dp140. West syndrome has been previously reported in two unrelated patients with Duchenne muscular dystrophy. Here, we report the third patient with West syndrome who had a novel hemizygous nonsense pathogenic variant in the exon 8 of the DMD gene c.811C>T, p.(Gln271*), suggesting West syndrome as part of the neuropsychiatric spectrum in Duchenne muscular dystrophy.


Assuntos
Distrofia Muscular de Duchenne/genética , Fenótipo , Espasmos Infantis/genética , Distrofina/genética , Epilepsia/genética , Éxons , Humanos , Lactente , Deficiência Intelectual/genética , Masculino , Mutação , Isoformas de Proteínas/genética
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