A carregar...
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...
Na minha lista:
| Publicado no: | J Med Case Rep |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2021
|
| Assuntos: | |
| Acesso em linha: | 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 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|