The Genotypic and Phenotypic Spectrum of BICD2 Variants in Spinal Muscular Atrophy

被引:22
|
作者
Koboldt, Daniel C. [1 ,2 ]
Waldrop, Megan A. [2 ,3 ,4 ]
Wilson, Richard K. [1 ,2 ]
Flanigan, Kevin M. [2 ,3 ,4 ]
机构
[1] Nationwide Childrens Hosp, Inst Genom Med, 700 Childrens Dr,WB2135, Columbus, OH 43205 USA
[2] Ohio State Univ, Dept Pediat, Columbus, OH 43210 USA
[3] Nationwide Childrens Hosp, Ctr Gene Therapy, Columbus, OH USA
[4] Ohio State Univ, Dept Neurol, Columbus, OH 43210 USA
关键词
MOTOR ADAPTER; MUTATIONS; DYNEIN; TRANSPORT; DYNACTIN; ARTHROGRYPOSIS; COMPLEX; FAMILY; LETHAL; CELLS;
D O I
10.1002/ana.25704
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The bicaudal D cargo adaptor 2 (BICD2) gene encodes a conserved cargo adaptor protein required for dynein-mediated transport. Inherited and de novo variants in BICD2 cause SMALED2 (spinal muscular atrophy lower extremity dominant 2), and a subset have recently been reported to cause severe, often lethal disease. However, a true genotype-phenotype correlation for BICD2 has not been performed, and cases described to date are scattered among at least 14 publications. In this review, we identify the characteristics of disease-causing variants in BICD2 that distinguish them from benign variation and perform genotype-phenotype correlations for 99 BICD2 variant carriers from 35 families. ANN NEUROL 2020;87:487-496
引用
收藏
页码:487 / 496
页数:10
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