A 1-month-old infant with chylomicronemia due to GPIHBP1 gene mutation treated by plasmapheresis

Chylomicronemia is a severe type of hypertriglyceridemia characterized by chylomicron accumulation that arises from a genetic defect in intravascular lipolysis. It requires urgent and proper management, because serious cases can be accompanied by pancreatic necrosis or persistent multiple organ fail...

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Detalles Bibliográficos
Autores principales: Jung, Mo Kyung, Jin, Juhyun, Kim, Hyun Ok, Kwon, Ahreum, Chae, Hyun Wook, Kang, Seok Jin, Kim, Duk Hee, Kim, Ho-Seong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pediatric Endocrinology 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5401827/
https://www.ncbi.nlm.nih.gov/pubmed/28443263
http://dx.doi.org/10.6065/apem.2017.22.1.68

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5401827/
https://www.ncbi.nlm.nih.gov/pubmed/28443263
http://dx.doi.org/10.6065/apem.2017.22.1.68

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