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Une cardiomyopathie révélant un déficit en carnitine palmitoyltransférase I: à propos d’un cas inhabituel
Carnitine palmitoyltransferase deficiencies (CPD) are rare and caused by a defect in fatty acid oxidation. We here report the case of a 10-year-old patient with no particular previous history presenting with acute dyspnea associated with productive cough, fever and impaired general condition. The pa...
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| Publicado no: | Pan Afr Med J |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The African Field Epidemiology Network
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7406460/ https://ncbi.nlm.nih.gov/pubmed/32821314 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2020.36.103.23646 |
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