Familial chylomicronemia syndrome: case reports of siblings with deletions of the GPIHBP1 gene
Abstract Background Familial chylomicronemia syndrome (FCS) is a rare monogenic form of severe hypertriglyceridemia, caused by mutations in genes involved in triglyceride metabolism. Herein, we report the case of a Korean family with familial chylomicronemia syndrome caused by compound heterozygous...
Tallennettuna:
| Päätekijät: | , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BMC
2024-04-01
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| Sarja: | BMC Endocrine Disorders |
| Aiheet: | |
| Linkit: | https://doi.org/10.1186/s12902-024-01574-9 |
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