Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience
Abstract Pontocerebellar hypoplasia (PCH) constitutes a heterogeneous neurodegenerative/neurodevelopmental disorder of the pons and cerebellum with onset in the prenatal period. Our study aimed to present different clinical and radiological manifestations of our genetically diagnosed PCH patients. M...
Main Authors: | Serap Bilge, Gülen Gül Mert, Özlem Hergüner, Duygu Özcanyüz, Sevcan Tuğ Bozdoğan, Ömer Kaya, Cengiz Havalı |
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Format: | Article |
Language: | English |
Published: |
BMC
2022-09-01
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Series: | Italian Journal of Pediatrics |
Subjects: | |
Online Access: | https://doi.org/10.1186/s13052-022-01349-9 |
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