Low-density lipoprotein apheresis in a pediatric patient of familial hypercholesterolemia: Primi experientia from a tertiary care center in North India

Familial hypercholesterolemia (FH) is an autosomal dominant disorder due to mutation of apolipoprotein-B receptor gene causing severe dyslipidemia. Lifestyle modification and medical treatment attenuate the disease progression, but as these fail to control the blood cholesterol levels, low-density l...

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Salvato in:
Dettagli Bibliografici
Pubblicato in:Asian J Transfus Sci
Autori principali: Dogra, Kanchan, Goyal, Alpesh, Khadgawat, Rajesh, Gupta, Yashdeep, Rout, Diptiranjan, Fulzele, Parag Prabhakar, Chaurasia, Rahul, Coshic, Poonam, Chatterjee, Kabita
Natura: Artigo
Lingua:Inglês
Pubblicazione: Medknow Publications & Media Pvt Ltd 2017
Soggetti:
Case Report
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5345283/
https://ncbi.nlm.nih.gov/pubmed/28316443
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0973-6247.200766
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