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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Detalhes bibliográficos
Publicado no:Ann Pediatr Endocrinol Metab
Main Authors: Jung, Mo Kyung, Jin, Juhyun, Kim, Hyun Ok, Kwon, Ahreum, Chae, Hyun Wook, Kang, Seok Jin, Kim, Duk Hee, Kim, Ho-Seong
Formato: Artigo
Idioma:Inglês
Publicado em: The Korean Society of Pediatric Endocrinology 2017
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5401827/
https://ncbi.nlm.nih.gov/pubmed/28443263
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6065/apem.2017.22.1.68
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