Evidence map›Paper›PMID 41446574›Full record

ArticleJCEM case reports2026

Familial Hypercholesterolemia in Ethiopia Using the Dutch Lipid Clinical Network Score: A Report of 3 Cases.

Kibret Enyew Belay, Dawit Girma Abebe, Minychel Wale Aynalem, Melaku Taye Amogne

Abstract readCase Reports
In one paragraph

Article in JCEM case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Kibret Enyew BelayDepartment of Internal Medicine, Division of Endocrinology and Metabolism, Bahir Dar University, Bahir Dar 6000, Ethiopia.ORCID https://orcid.org/0000-0002-7943-0147
Dawit Girma AbebeDepartment of Internal Medicine, ALERT Comprehensive Specialized Hospital, Addis Ababa 4010, Ethiopia.
Minychel Wale AynalemArmauer Hansen Research Institute, Addis Ababa 1005, Ethiopia.
Melaku Taye AmogneDepartment of Internal Medicine, Division of Endocrinology and Metabolism, Addis Ababa University, Addis Ababa 1000, Ethiopia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Familial hypercholesterolemia is a common genetic disease caused by mutation of 1 or more of the genes critical for low-density lipoprotein cholesterol catabolism. It is associated with markedly increased risk of premature atherosclerotic cardiovascular disease. It remains underdiagnosed, especially in low- and middle-income countries like Ethiopia. In this report, we present the first case series of adults phenotypically diagnosed with heterozygous familial hypercholesterolemia in Ethiopia using the Dutch Lipid Clinical Network Score. Our findings underscore the importance of early detection and timely intervention to mitigate cardiovascular risk in affected individuals.

Indexed as

Dutch Lipid Clinical Network ScoreEthiopiafamilial hypercholesterolemiagenetic dyslipidemiapremature cardiovascular diseasetendon xanthoma

Identifiers

PMID41446574
PMCPMC12723231

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.