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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...

Ausführliche Beschreibung

Gespeichert in:
Hauptverfasser: Luyao Jin, Shuling Chen, Ying Liu, Renyi She, Wei Jiang
Format: Artigo
Sprache:Inglês
Veröffentlicht: Wiley 2026-07-01
Schriftenreihe:Molecular Genetics & Genomic Medicine
Schlagworte:
ataxia
cerebellar atrophy
children
gene mutation
hereditary
Online-Zugang:https://doi.org/10.1002/mgg3.70258
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