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Article

The management of familial hypercholesterolaemia in Morocco.

Acta cardiologica - 1 Oct 2006

El Messal Mariame, Aït Chihab Karima, Chater Rachid, Loutfi Mohamed, Kettani Anas, Hafidi Aïcha, Adlouni Ahmed

Abstract excerpt

Familial hypercholesterolaemia (FH) is an autosomal dominant disorder characterized by high levels of low-density lipoprotein cholesterol (LDL-C) as a result of mutations that impair their removal from plasma.The clinical consequence is a high risk of premature cardiovascular disease. Because of the extreme risk of mortality and morbidity, diagnosis, recruitment and management of FH patients must be one of the...

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Share to Apolipoproteins B
Share to Cholesterol, LDL
Share to Hyperlipoproteinemia Type II

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 17117756
DOI: 10.2143/AC.61.5.2017771

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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