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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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Detalles Bibliográficos
Autores principales:	Dogra, Kanchan, Goyal, Alpesh, Khadgawat, Rajesh, Gupta, Yashdeep, Rout, Diptiranjan, Fulzele, Parag Prabhakar, Chaurasia, Rahul, Coshic, Poonam, Chatterjee, Kabita
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2017
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5345283/ https://www.ncbi.nlm.nih.gov/pubmed/28316443 http://dx.doi.org/10.4103/0973-6247.200766

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