Evidence map›Paper›PMID 39905508›Full record

ArticleJournal of medical case reports2025

Rheumatoid-like hand deformities and aortic valve disease in a 13-year-old girl with homozygous familial hypercholesterolemia: a case report.

Anjuman Ara Rahman, Abhijit Datta, Kamal Uddin Ahmed, Anindita Das Barshan, Mohammad Jahid Hasan

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Article in Journal of medical case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Anjuman Ara RahmanBangabandhu Sheikh Mujib Medical College Hospital, Faridpur, Bangladesh.
Abhijit DattaBangabandhu Sheikh Mujib Medical College Hospital, Faridpur, Bangladesh.
Kamal Uddin AhmedDepartment of Cardiology, Bangabandhu Sheikh Mujib Medical College Hospital, Faridpur, Bangladesh.
Anindita Das BarshanTropical Disease and Health Research Center, Dhaka, 1100, Bangladesh.
Mohammad Jahid HasanTropical Disease and Health Research Center, Dhaka, 1100, Bangladesh. dr.jahid61@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFamilial hypercholesterolemia is an autosomal dominant disorder characterized by elevated serum low-density lipoprotein cholesterol levels, tendon xanthomas, and an increased risk of atherosclerotic heart disease. Diagnosing familial hypercholesterolemia at an early age is crucial owing to its potential to lead to severe cardiovascular complications, including coronary heart disease and aortic valve disease. Early detection allows timely intervention, such as lifestyle modifications and pharmacological treatments, which can significantly reduce these risks. CASE PRESENTATION: In this case report, we present a case of familial hypercholesterolemia in a 13-year-old Bangladeshi girl residing in Faridpur, Bangladesh. The patient presented with a distinctive clinical profile, including the presence of tendon xanthoma in the hands and cutaneous xanthoma in the elbow, knee, and buttocks, as well as recent development of aortic valvular diseases. In addition, she experienced joint deformity in both hands, mimicking rheumatoid arthritis, which is uncommon. The patient was diagnosed and underwent treatment through both lifestyle changes and medication. Moreover, her family received genetic counseling, and she was scheduled for regular follow-up.

conclusionThis case underscores the significance of identifying important physical signs in the diagnosis and management of familial hypercholesterolemia, particularly in settings where genetic testing may be limited. Moreover, the unique coexistence of familial hypercholesterolemia with hand joint deformity and aortic valvular heart disease serves as a clinical clue that can facilitate diagnosis and appropriate therapeutic interventions. A high index of suspicion is essential for timely diagnosis and tailored management, thus reducing the burden of atherosclerotic heart disease in affected individuals.

Indexed as

Aortic Valve DiseaseHandHyperlipoproteinemia Type IIAdolescentDiagnosis, DifferentialFemaleHomozygoteHumansXanthomatosisAortic valve diseaseAutosomal dominant disorderCase reportFamilial hypercholesterolemiaTendon xanthoma

Identifiers

PMID39905508
PMCPMC11792261

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