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Familial chylomicronemia syndrome: a case report
BACKGROUND: Familial chylomicronemia is an extremely rare disease. Lipoprotein lipase deficiency, lipoprotein defect or lipoprotein receptor defect are the main genetic causes of familial chylomicronemia. CASE PRESENTATION: We report a rare case of hypertriglyceridemia which was diagnosed at 24 days...
Gardado en:
| Publicado en: | J Med Case Rep |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2021
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7791813/ https://ncbi.nlm.nih.gov/pubmed/33419463 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13256-020-02609-0 |
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