Back to Search
Start Over
The Genotypic and Phenotypic Spectrum of BICD2 Variants in Spinal Muscular Atrophy
- Source :
- Annals of Neurology. 87:487-496
- Publication Year :
- 2020
- Publisher :
- Wiley, 2020.
-
Abstract
- 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.
- Subjects :
- 0301 basic medicine
Genotype
Disease
Spinal Muscular Atrophies of Childhood
Biology
medicine.disease_cause
Severity of Illness Index
03 medical and health sciences
0302 clinical medicine
medicine
Humans
Mobility Limitation
Gene
Genetic Association Studies
Genetics
Mutation
Muscle Weakness
Signal transducing adaptor protein
Spinal muscular atrophy
medicine.disease
BICD2
Phenotype
Muscular Atrophy
030104 developmental biology
Neurology
Neurology (clinical)
Respiratory Insufficiency
Microtubule-Associated Proteins
030217 neurology & neurosurgery
Subjects
Details
- ISSN :
- 15318249 and 03645134
- Volume :
- 87
- Database :
- OpenAIRE
- Journal :
- Annals of Neurology
- Accession number :
- edsair.doi.dedup.....39575670cf7912ee98bc2bcba5a75e4d
- Full Text :
- https://doi.org/10.1002/ana.25704