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Article

Exploring the phenotypic and genotypic spectrum of spinal muscular atrophy in Bangladeshi children.

BMC neurology - 8 May 2026

Parvin Jobaida, Khan Husnea Ara, Saha Narayan Chandra, Hoque Seikh Azimul, Hossain Mohammad Monir, Saha Dipa, Shams Nusrat

Abstract excerpt

Spinal muscular atrophy (SMA) is a monogenic neuromuscular disorder caused by SMN1 gene deletion and classified by clinical severity. The objective of this study was to evaluate the genotypic and phenotypic spectrum in SMA in Bangladeshi children.This cross-sectional prospective study was conducted in Pediatric Neurology Department, National Institute of Neurosciences and Hospital of Bangladesh from January 2019...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 42104248
DOI: 10.1186/s12883-026-04946-x
PMCID: PMC13321646

Genes

SMN2
SMN1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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