Familial hypercholesterolemia (FH) is a genetic disease presented by high levels of serum low density lipoprotein (LDL), xanthomas and early coronary artery disease (CAD). The diagnosis of Homozygous Familial Hypercholesterolemia (HoFH) is based on a family history of elevated cholesterol, persistent high LDL levels despite maximum medical treatment and the development of xanthomas and early atherosclerotic cardiac lesions such as aortic stenosis. Management of HoFH patients requires lifestyle modifications and medical therapy
| Published in | American Journal of Internal Medicine (Volume 2, Issue 2) |
| DOI | 10.11648/j.ajim.20140202.15 |
| Page(s) | 34-40 |
| Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
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Copyright © The Author(s), 2014. Published by Science Publishing Group |
Familial Hypercholesterolemia (FH), Homozygous Familial Hypercholesterolemia (HoFH), Xanthomas, Genetic Disease
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APA Style
Vinod Kumar Khurana, Raj Kumar Mehta, Kapil Chandra. (2014). Homozygous Familial Hypercholesterolemia: Case report and Review of Literature. American Journal of Internal Medicine, 2(2), 34-40. https://doi.org/10.11648/j.ajim.20140202.15
ACS Style
Vinod Kumar Khurana; Raj Kumar Mehta; Kapil Chandra. Homozygous Familial Hypercholesterolemia: Case report and Review of Literature. Am. J. Intern. Med. 2014, 2(2), 34-40. doi: 10.11648/j.ajim.20140202.15
AMA Style
Vinod Kumar Khurana, Raj Kumar Mehta, Kapil Chandra. Homozygous Familial Hypercholesterolemia: Case report and Review of Literature. Am J Intern Med. 2014;2(2):34-40. doi: 10.11648/j.ajim.20140202.15
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Download@article{10.11648/j.ajim.20140202.15,
author = {Vinod Kumar Khurana and Raj Kumar Mehta and Kapil Chandra},
title = {Homozygous Familial Hypercholesterolemia: Case report and Review of Literature},
journal = {American Journal of Internal Medicine},
volume = {2},
number = {2},
pages = {34-40},
doi = {10.11648/j.ajim.20140202.15},
url = {https://doi.org/10.11648/j.ajim.20140202.15},
eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajim.20140202.15},
abstract = {Familial hypercholesterolemia (FH) is a genetic disease presented by high levels of serum low density lipoprotein (LDL), xanthomas and early coronary artery disease (CAD). The diagnosis of Homozygous Familial Hypercholesterolemia (HoFH) is based on a family history of elevated cholesterol, persistent high LDL levels despite maximum medical treatment and the development of xanthomas and early atherosclerotic cardiac lesions such as aortic stenosis. Management of HoFH patients requires lifestyle modifications and medical therapy},
year = {2014}
}
TY - JOUR T1 - Homozygous Familial Hypercholesterolemia: Case report and Review of Literature AU - Vinod Kumar Khurana AU - Raj Kumar Mehta AU - Kapil Chandra Y1 - 2014/04/20 PY - 2014 N1 - https://doi.org/10.11648/j.ajim.20140202.15 DO - 10.11648/j.ajim.20140202.15 T2 - American Journal of Internal Medicine JF - American Journal of Internal Medicine JO - American Journal of Internal Medicine SP - 34 EP - 40 PB - Science Publishing Group SN - 2330-4324 UR - https://doi.org/10.11648/j.ajim.20140202.15 AB - Familial hypercholesterolemia (FH) is a genetic disease presented by high levels of serum low density lipoprotein (LDL), xanthomas and early coronary artery disease (CAD). The diagnosis of Homozygous Familial Hypercholesterolemia (HoFH) is based on a family history of elevated cholesterol, persistent high LDL levels despite maximum medical treatment and the development of xanthomas and early atherosclerotic cardiac lesions such as aortic stenosis. Management of HoFH patients requires lifestyle modifications and medical therapy VL - 2 IS - 2 ER -
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