Unmasking a rare genetic mutation: The importance of genetic testing in refractory hypertriglyceridemia-Reference-Cited by-同舟云学术

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Unmasking a rare genetic mutation: The importance of genetic testing in refractory hypertriglyceridemia

Published:2024-08 Issue: Volume: Page:
ISSN:2376-0605
Container-title:AACE Clinical Case Reports
language:en
Short-container-title:AACE Clinical Case Reports

Author:

Theodoropoulos Panagiotis^ORCID,Fanaropoulou Nina Maria,Manessis Anastasios

Publisher

Elsevier BV

Reference15 articles.

1. Management of hypertriglyceridemia;Simha;BMJ,2020

2. Familial chylomicronemia syndrome: A rare but devastating autosomal recessive disorder characterized by refractory hypertriglyceridemia and recurrent pancreatitis;Chyzhyk;Trends Cardiovasc Med,2020

3. Familial Chylomicronemia Syndrome With a Novel Homozygous LPL Mutation Identified in Three Siblings in Their 50s;Ueda;Ann Intern Med,2020

4. Familial chylomicronemia syndrome: importance of diagnostic vigilance;Ueda;Transl Pediatr,2022

5. Chylomicronemia: Differences between familial chylomicronemia syndrome and multifactorial chylomicronemia;Paquette;Atherosclerosis,2019

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