Cover image of the article: A Report of Two Children with Severe Homozygous Familial Hypercholesterolemia

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A Report of Two Children with Severe Homozygous Familial Hypercholesterolemia

Authors

Noormohammad Noori1, Ghasem Miri-Aliabad1,*, mehdi jahantigh2
1Department of Pediatrics, Children and Adolescent Health Research Center, Zahedan University of Medical Sciences, Zahedan, Iran
2Department of Pathology, Zahedan University of Medical Sciences and Health Services, Zahedan, Iran
*Corresponding Author: Department of Pediatrics, Children and Adolescent Health Research Center, Zahedan University of Medical Sciences, Zahedan, Iran Email: gh_miri@yahoo.com

Zahedan Journal of Research in Medical Sciences:Vol. 15, issue 4; e93043
Published online:Nov 05, 2012
Article type:Case Report
Received:Apr 04, 2012
Accepted:Jun 27, 2012
How to Cite:Noori N, Miri-Aliabad G, jahantigh M. A Report of Two Children with Severe Homozygous Familial Hypercholesterolemia. Zahedan J Res Med Sci. 2013;15(4):e93043. doi:

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.

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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.

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