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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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Hoofdauteurs: Luyao Jin, Shuling Chen, Ying Liu, Renyi She, Wei Jiang
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Wiley 2026-07-01
Reeks:Molecular Genetics & Genomic Medicine
Onderwerpen:
ataxia
cerebellar atrophy
children
gene mutation
hereditary
Online toegang:https://doi.org/10.1002/mgg3.70258
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