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...
Gorde:
| Egile Nagusiak: | , , , , , , |
|---|---|
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BMC
2024-04-01
|
| Saila: | BMC Endocrine Disorders |
| Gaiak: | |
| Sarrera elektronikoa: | https://doi.org/10.1186/s12902-024-01574-9 |
| Etiketak: |
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!
|