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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Ann Pediatr Endocrinol Metab
Autors principals: Jung, Mo Kyung, Jin, Juhyun, Kim, Hyun Ok, Kwon, Ahreum, Chae, Hyun Wook, Kang, Seok Jin, Kim, Duk Hee, Kim, Ho-Seong
Format: Artigo
Idioma:Inglês
Publicat: The Korean Society of Pediatric Endocrinology 2017
Matèries:
Case Report
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars