Correlation Analysis of Clinical, Imaging, and Genetic Etiologies in Pediatric Hereditary Cerebellar Atrophy: A Single‐Center Study

ABSTRACT Objective To investigate the associations among clinical features, neuroimaging findings, and genetic data in children with hereditary cerebellar atrophy (CA). Method A cohort of 102 pediatric patients diagnosed with hereditary CA was enrolled at the Children's Hospital of Chongqing Medical...

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Detalhes bibliográficos

Principais autores:	Luyao Jin, Shuling Chen, Ying Liu, Renyi She, Wei Jiang
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Wiley 2026-07-01
coleção:	Molecular Genetics & Genomic Medicine
Assuntos:	ataxia cerebellar atrophy children gene mutation hereditary
Acesso em linha:	https://doi.org/10.1002/mgg3.70258
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