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...

Descripción completa

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

Internet

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

Ejemplares similares