Evidence map›Paper›PMID 40510075›Full record

ArticleCureus2025

Unveiling Fahr's Syndrome in a Child: A Case Linked to Congenital Hypoparathyroidism.

Ghizlane Kassal, Rabiy Elqadiri, Soumia Mghar, Houda Nassih, Aicha Abourrahouat, Sara Ouassil, Imane Aitsab

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. 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

7 authors.

Ghizlane KassalMother and Child Department, General Pediatrics, University Hospital Center, Mohammed VI, Marrakech, MAR.
Rabiy ElqadiriMother and Child Department, General Pediatrics, University Hospital Center, Mohammed VI, Marrakech, MAR.
Soumia MgharMother and Child Department, General Pediatrics, University Hospital Center, Mohammed VI, Marrakech, MAR.
Houda NassihMother and Child Department, General Pediatrics, University Hospital Center, Mohammed VI, Marrakech, MAR.
Aicha AbourrahouatMother and Child Department, General Pediatrics, University Hospital Center, Mohammed VI, Marrakech, MAR.
Sara OuassilRadiology Department, University Hospital Center, Mohammed VI, Marrakech, MAR.
Imane AitsabMother and Child Department, General Pediatrics, University Hospital Center, Mohammed VI, Marrakech, MAR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fahr's syndrome is a rare neurological disorder marked by unusual calcium deposits in specific brain regions. Its occurrence is linked to various underlying causes, including hormonal imbalances, genetic predispositions, infections affecting the central nervous system, and exposure to certain toxic substances. We describe a pediatric case of Fahr's syndrome linked to hypoparathyroidism, presenting with seizures and developmental delays. Suspicion of this diagnosis was raised due to anamnestic, clinical, and laboratory findings and confirmed after the cerebral computed tomography (CT) scan showed brain calcifications. Emphasizing the necessity of early identification, this case underscores the value of clinical and biological markers in guiding diagnosis. Additionally, it highlights the essential role of imaging techniques in confirming the presence of brain calcifications and aiding effective management.

Indexed as

childhypocalcemiahypoparathyroidismpsychomotor delaysecondary fahr´s syndrome

Identifiers

PMID40510075
PMCPMC12159691

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Registered trials

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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.