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Zellweger syndrome: A cause of neonatal hypotonia and seizures
Zellweger syndrome, a paradigm of human peroxisomal disorders is characterized by dysmorphic features, hypotonia, severe neuro-developmental delay, hepatomegaly, renal cysts, sensorineural deafness and retinal dysfunction. This is a case report of a baby boy born with facial dysmorphism, profound hy...
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| Publicado no: | Sudan J Paediatr |
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| Autor principal: | |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Sudanese Association of Pediatricians
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4949836/ https://ncbi.nlm.nih.gov/pubmed/27493320 |
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