A novel Gly436Glu variant in the LPL gene identified in a Saudi Arabian patient with severe hypertriglyceridemia and recurrent pancreatitis

Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive disorder characterized by severe hypertriglyceridemia and recurrent pancreatitis, often manifesting in childhood. The condition results from variants in the lipoprotein lipase (LPL) gene, which lead to impaired fat metabolism. We...

Full description

Saved in:
Bibliographic Details
Main Authors: Dena A. Nuwaylati, Hussam Daghistani, Noor Ahmad Shaik, Zuhier A. Awan
Format: Article
Language:English
Published: Sungkyunkwan University School of Medi 2024-12-01
Series:Precision and Future Medicine
Subjects:
Online Access:http://pfmjournal.org/upload/pdf/pfm-2024-00163.pdf
Tags: Add Tag
No Tags, Be the first to tag this record!