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Pontocerebellar Hypoplasia Diagnosed on Autopsy: A Case Report
Pontocerebellar hypoplasia (PCH) is a diverse group of autosomal recessive genetic conditions presenting with hypoplastic changes in the brainstem, cerebellum, and spinal cord. It clinically manifests with neurological symptoms, respiratory failure, and often in a combination with other malformation...
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| Pubblicato in: | Cureus |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Cureus
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7301432/ https://ncbi.nlm.nih.gov/pubmed/32566419 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.8178 |
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