Evidence map›Paper›PMID 41984085›Full record

ArticleJournal of clinical hypertension (Greenwich, Conn.)2026

Severe Hypertension and Hematologic Abnormalities in Pseudoxanthoma Elasticum: A Pediatric Case Report.

Hana Flogelova, Dagmar Pospisilova, Lenka Bakaj-Zbrozkova, Lucie Sochorcova, Jirina Manakova, Eva Kriegova, Pavla Koralkova, Katarina Hlusickova Kapralova, Monika Horvathova

Abstract readCase Reports
In one paragraph

Article in Journal of clinical hypertension (Greenwich, Conn.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

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

9 authors.

Hana FlogelovaDepartment of Pediatrics, Faculty of Medicine and Dentistry, Palacky University and University Hospital Olomouc, Olomouc, Czech Republic.ORCID 0000-0003-2995-5735
Dagmar PospisilovaDepartment of Pediatrics, Faculty of Medicine and Dentistry, Palacky University and University Hospital Olomouc, Olomouc, Czech Republic.ORCID 0000-0002-2974-9205
Lenka Bakaj-ZbrozkovaDepartment of Radiology, Faculty of Medicine and Dentistry, Palacky University and University Hospital Olomouc, Olomouc, Czech Republic.ORCID 0009-0007-6058-6655
Lucie SochorcovaDepartment of Biology, Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic.ORCID 0000-0003-1737-8125
Jirina ManakovaDepartment of Immunology, Faculty of Medicine and Dentistry, Palacky University and University Hospital Olomouc, Olomouc, Czech Republic.
Eva KriegovaDepartment of Immunology, Faculty of Medicine and Dentistry, Palacky University and University Hospital Olomouc, Olomouc, Czech Republic.ORCID 0000-0002-8969-4197
Pavla KoralkovaDepartment of Biology, Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic.ORCID 0000-0001-7970-1501
Katarina Hlusickova KapralovaDepartment of Biology, Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic.ORCID 0000-0001-6235-2915
Monika HorvathovaDepartment of Biology, Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic.ORCID 0000-0003-3857-8986

Funding

Internal grant of the Faculty Hospital Olomouc MHCZ-DRO (FNOI, 00098892)
6 · The paper itself

Abstract

Pseudoxanthoma elasticum (PXE) is a rare autosomal recessive disorder caused by pathogenic variants in ABCC6, leading to progressive calcification of elastic fibers. Although PXE typically presents in adolescence with dermatologic or ocular manifestations, early vascular involvement, including pediatric hypertension, is increasingly recognized. We report a 3-year-old boy referred for evaluation of persistent erythrocytosis of unclear etiology. Clinical, biochemical, and hematologic assessments revealed intermittent reticulocytosis, normal oxygen saturation, and suppressed/normal erythropoietin levels. Long-term zinc supplementation initiated in infancy for suspected dermatitis enteropathica preceded the onset of erythrocytosis. At age eight, severe systemic hypertension was diagnosed together with medullary nephrocalcinosis and splenic and pancreatic calcifications. Imaging excluded renal artery stenosis. Whole-exome sequencing identified compound heterozygous pathogenic ABCC6 variants, establishing the diagnosis of PXE. Ophthalmologic examination revealed peau d'orange. Blood pressure control required combination antihypertensive therapy and was associated with partial normalization of red blood cell (RBC) parameters and a marked increase in plasma renin activity. RBC enzymatic profiling demonstrated metabolic adaptations consistent with oxidative stress. This case illustrates an unusual clinical presentation of PXE in early childhood. We propose that erythrocytosis, potentially promoted by zinc supplementation, may have contributed to early vascular stress and hypertension. Later, renal microvascular calcification and renin-angiotensin-aldosterone system activation may have contributed to the persistence of elevated RBC counts despite low erythropoietin. These observations suggest that PXE may be considered in the differential diagnosis of children with unexplained hypertension, particularly when additional systemic findings are present.

Indexed as

HypertensionPolycythemiaPseudoxanthoma ElasticumAntihypertensive AgentsATP-Binding Cassette, Sub-Family C ProteinsChild, PreschoolExome SequencingHumansMaleZincABCC6 protein, humanAntihypertensive AgentsATP-Binding Cassette, Sub-Family C ProteinsZincABCC6ectopic mineralizationerythrocytosispediatric hypertensionpseudoxanthoma elasticum

Identifiers

PMID41984085
PMCPMC13082210

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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.