Evidence map›Paper›PMID 42528835›Full record

ArticleClinical case reports2026

Clinical and Radiological Features Suggestive of Mucopolysaccharidosis in Two Siblings From Sudan: A Case Series.

Alaa Bella, Mumen Abdalazim Dafallah, Ashraf Yousif Fadlalla, Bothaina Faisal Elmardi, Yomna Mohialdin Alataya, Abdalla Abdelmahmoud Abdalla, Mohammed Almeldin Ahmed Ibrahim, Mawada Faisal Nugud, Salah Elamin Ahmed Babiker, Hiba Faroug Al Amin and 2 more

Abstract read
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In one paragraph

Article in Clinical 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.

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

12 authors.

Alaa BellaInternal Medicine Department University of Gezira Wad Madani Al Jazīrah Sudan.ORCID https://orcid.org/0009-0009-3839-6331
Mumen Abdalazim DafallahInternal Medicine Department Sudan Medical Specialization Board Wad Medani Al Jazīrah Sudan.ORCID https://orcid.org/0000-0002-4300-9481
Ashraf Yousif FadlallaInternal Medicine Department University of Gezira Wad Madani Al Jazīrah Sudan.ORCID https://orcid.org/0009-0001-5621-2892
Bothaina Faisal ElmardiInternal Medicine Department University of Gezira Wad Madani Al Jazīrah Sudan.ORCID https://orcid.org/0009-0002-9753-3526
Yomna Mohialdin AlatayaInternal Medicine Department University of Gezira Wad Madani Al Jazīrah Sudan.ORCID https://orcid.org/0009-0007-9589-5415
Abdalla Abdelmahmoud AbdallaInternal Medicine Department University of Gezira Wad Madani Al Jazīrah Sudan.ORCID https://orcid.org/0009-0009-2092-3295
Mohammed Almeldin Ahmed IbrahimInternal Medicine Department University of Blue Nile Damazeen Sudan.
Mawada Faisal NugudInternal Medicine Department University of Gezira Wad Madani Al Jazīrah Sudan.ORCID https://orcid.org/0009-0006-2710-5015
Salah Elamin Ahmed BabikerInternal Medicine Department University of Gezira Wad Madani Al Jazīrah Sudan.
Hiba Faroug Al AminInternal Medicine Department Sinnar University Sinnar Sudan.
Safaa Ayoub Yousif MohammedInternal Medicine Department University of Gezira Wad Madani Al Jazīrah Sudan.
Moawia Elbalal MohammedInternal Medicine Department University of Gezira Wad Madani Al Jazīrah Sudan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mucopolysaccharidosis should be suspected in patients presenting with multisystem involvement, including coarse facial features, skeletal abnormalities, and progressive organ dysfunction, particularly in resource-limited settings where delayed diagnosis is common. Early clinical recognition is crucial, as timely diagnosis can facilitate appropriate supportive care, genetic counseling, ultimately improving quality of life.

Indexed as

case seriesinherited lysosomal storage disordersmucopolysaccharidosisSudan

Identifiers

PMID42528835
PMCPMC13415741

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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.