Zahedan Journal of Research in Medical Sciences
The Official Journal of Zahedan University of Medical Sciences
Image Credit:Zahedan J Res Med Sci
Outline
A Report of Two Children with Severe Homozygous Familial Hypercholesterolemia
Authors
Abstract
Familial hypercholesterolemia (FH) is an autosomal disorder that causes severe elevations in total cholesterol and low- density lipoprotein. FH is one of the primary risk factors for premature coronary artery disease in children and adults which requires early diagnosis and appropriate medical intervention. In this article, we report two cases of homozygous familial hypercholesterolemia.
References
- 1.The References of this article are available on the PDF file.
Copyright
© 2013, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.
Similar Articles
The First Report of GAC AAC Mutation in Familial Hypercholesterolemia in Khuzestan
Nikkhooy M, Foroughmand AM, Galehdari H, Yazdankhah S. The First Report of GAC>AAC Mutation in Familial Hypercholesterolemia in Khuzestan. Zahedan J Res Med Sci. 2018;20(8):e6642. doi: https://doi.org/10.5812/zjrms.6642
Coronary Artery Revascularization in a young adult with Solitary Coronary Aneurysm probably secondary to childhood Kawasaki Disease
Baghaei R, Rezaei M. Coronary Artery Revascularization in a young adult with Solitary Coronary Aneurysm probably secondary to childhood Kawasaki Disease. Multidiscip Cardio Annal. 2010;3(5):e8759. doi:
Familial Hemophagocytic Lymphohistiocytosis Type 3: Early Disease Onset and Unusual Manifestation in Sibling Cases
Huang J, Jiang L, Wu X, Cheng Y, Chen C, et al. Familial Hemophagocytic Lymphohistiocytosis Type 3: Early Disease Onset and Unusual Manifestation in Sibling Cases. Inn J Pediatr. 2019;29(2):e82160. doi: https://doi.org/10.5812/ijp.82160
Correlation of premature coronary artery disease in parents with dyslipidemia in their children
Masoumi M, Jalili Z, Sabzi F, moradi B, Abdoli G, et al. Correlation of premature coronary artery disease in parents with dyslipidemia in their children. J Kermanshah Univ Med Sci. 2003;7(2):e81210. doi:
Investigation of PCSK9 Gene Polymorphisms in Two Iranian Ethnic Groups with Coronary Artery Disease in Fars Province
Zibaeenezhad MJ, Yavarian M, Fathzadeh M, Heydari Kamrodi M, Fattahi Mofrad M, et al. Investigation of PCSK9 Gene Polymorphisms in Two Iranian Ethnic Groups with Coronary Artery Disease in Fars Province. Int Cardiovasc Res J. 2020;14(2):e100140. doi:
More by these authors
- Scopus by DOI: 0
Last Update: 2 weeks ago
- Scopus by Title: 0
Last Update: 2 weeks ago
- Scopus by Title (Ref): 0
Last Update: 2 weeks ago
- CrossRef: 0
Last Update: 7 hours ago
- OpenAlex: 0
Last Update: 10 hours ago
- OpenCitations: 0
Last Update: 5 days ago