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...
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| Main Authors: | , , , , , , |
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| Format: | Book |
| Published: |
BMC,
2022-09-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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