Familial chylomicronemia syndrome due to a heterozygous deletion of the chromosome 8 treated with the apoCIII inhibitor volanesorsen: A case report

RATIONALE: Familial chylomicronemia syndrome is a congenital, severe form of hypertriglyceridemia associated with increased risk of acute pancreatitis. Treatment options are limited. PATIENT CONCERNS: A 52-year-old woman was referred with recurrent pancreatitis and severe hypertriglyceridemia to our...

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Detalles Bibliográficos
Autores principales: Tünnemann-Tarr, Adrienn, Scharnagl, Hubert, Katzmann, Julius L., Stürzebecher, Paulina, Laufs, Ulrich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
3500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8542157/
https://www.ncbi.nlm.nih.gov/pubmed/34678899
http://dx.doi.org/10.1097/MD.0000000000027573

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8542157/
https://www.ncbi.nlm.nih.gov/pubmed/34678899
http://dx.doi.org/10.1097/MD.0000000000027573

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