Evidence map›Paper›PMID 42725152›Full record

ArticleEuropean journal of case reports in internal medicine2026

Familial Hypocalciuric Hypercalcemia and Early Severe Aortic Stenosis in A Patient with two Different Heart Failure Episodes.

Ana Margarida Fonseca, Mariana Lobo Oliveira, Ana Cordeiro Gomes, Luis Nogueira-Silva, Joana Pereira, Jorge Almeida, Patrícia Lourenço

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Article in European journal of case reports in internal medicine, 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Ana Margarida FonsecaInternal Medicine Department, Centro Hospitalar e Universitário de São João, Porto, Portugal.
Mariana Lobo OliveiraInternal Medicine Department, Centro Hospitalar e Universitário de São João, Porto, Portugal.
Ana Cordeiro GomesInternal Medicine Department, Centro Hospitalar e Universitário de São João, Porto, Portugal.
Luis Nogueira-SilvaInternal Medicine Department, Centro Hospitalar e Universitário de São João, Porto, Portugal.
Joana PereiraInternal Medicine Department, Centro Hospitalar e Universitário de São João, Porto, Portugal.
Jorge AlmeidaInternal Medicine Department, Centro Hospitalar e Universitário de São João, Porto, Portugal.
Patrícia LourençoInternal Medicine Department, Centro Hospitalar e Universitário de São João, Porto, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Familial hypocalciuric hypercalcemia (FHH) is a rare hereditary cause of mild hypercalcemia that usually follows a benign clinical course. Calcific aortic stenosis (AS) in a trileaflet aortic valve is uncommon before 65 years of age. Emerging evidence suggests that disturbances in calcium metabolism may contribute to aortic valve calcification. Case description: A 58-year-old woman presented in 2012 with acute heart failure (HF) and left ventricular ejection fraction (LVEF) of 32%. Coronary angiography was normal, and endomyocardial biopsy was not suggestive of myocarditis. She achieved complete recovery with guideline-directed medical therapy, consistent with resolved idiopathic cardiomyopathy. Echocardiography at that time showed only mild aortic valve thickening. She had chronic mild hypercalcemia consistent with FHH, supported by family history, normal parathyroid hormone levels, and fractional excretion of calcium <1%. Genetic testing was negative. During the following decade, progressive aortic valve calcification was documented. In 2023, echocardiography revealed severe AS with a functionally bicuspid valve (peak/mean gradients 105/69 mmHg; valve area 0.5 cm Conclusion: This case suggests a possible association between FHH and accelerated valvular calcification leading to premature severe AS. It is also notable for two separate HF episodes caused by different aetiologies: reversible cardiomyopathy initially, followed a decade later by severe AS. Although FHH is generally considered benign, chronic hypercalcemia may justify closer long-term cardiovascular surveillance. LEARNING POINTS: Familial hypocalciuric hypercalcemia may be associated with accelerated valvular calcification and premature severe aortic stenosis.Serial imaging over 10 years documented progression from mild valve thickening to severe calcific aortic stenosis.The case describes two distinct episodes of heart failure caused by different underlying mechanisms.

Indexed as

aortic valve calcificationaortic valve stenosisfamilial hypocalciuric hypercalcemiaheart failureHypercalcemia

Identifiers

PMID42725152
PMCPMC13561145

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