Third case of Duchenne muscular dystrophy and West syndrome: Expanding the spectrum of the DMD neuropsychiatric phenotype

被引:3
|
作者
Pena-Padilla, Christian [1 ]
Romero-Valenzuela, Ivon [1 ]
Baldomero-Lopez, Alejandra [1 ]
Karen Sandoval-Talamantes, Ana [2 ]
Castellanos-Gonzalez, Abril [3 ]
Nagy, Peter L. [4 ]
Kelly, Rebecca R. [4 ]
Roman Corona-Rivera, Jorge [1 ,5 ]
机构
[1] Dr Juan I Menchaca Civil Hosp Guadalajara, Ctr Registry & Res Congenital Anomalies CRIAC, Serv Genet, Pediat Div, Guadalajara, Jalisco, Mexico
[2] Univ Hosp La Paz, Inst Med & Mol Genet, Unit Struct & Funct Genom, Madrid, Spain
[3] Puerta Hierro Med Ctr, Serv Pediat Neurol, Zapopan, Mexico
[4] Cardona Medina Salvador Milenia Labs, MNG Labs, Atlanta, GA USA
[5] Univ Guadalajara, Dr Enrique Corona Rivera Inst Human Genet, Hlth Sci Univ Ctr, Dept Mol Biol & Genom, Siena Mojada 950,Bldg P,Level 2, Guadalajara 44340, Jalisco, Mexico
关键词
Duchenne muscular dystrophy; West syndrome; Epilepsy; Dystrophin isoforms; DP71;
D O I
10.1016/j.nmd.2021.02.004
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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. (C) 2021 Elsevier B.V. All rights reserved.
引用
收藏
页码:462 / 465
页数:4
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