Evidence map›Paper›PMID 42465820›Full record

ArticleThe Pan African medical journal2026

[Cross-sectional study on medical coverage for children with Down syndrome in Morocco: case study of the dysmorphology unit of the paediatrics 2 department at Ibn Sina University Hospital in Rabat].

Meriem Benadada, Saida Naji, Nada Bennani Mechita, Samia El Hilali, Yassine Sarboute, Majdouline Obtel, Asmaa Mdaghri Alaoui

Abstract readEnglish Abstract
In one paragraph

Article in The Pan African medical journal, 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

7 authors.

Meriem BenadadaÉquipe de Recherche sur les Anomalies Congénitales, Faculté de Médecine et de Pharmacie, Université Mohammed V, Rabat, Maroc.
Saida NajiLaboratoire de Recherche en Compétitivité Économique et Performance Managériale, Faculté des Sciences Juridiques, Économiques et Sociales de Souissi, Université Mohammed V, Rabat, Maroc.
Nada Bennani MechitaUnité de Dysmorphologie, Service de Pédiatrie 2, Hôpital d'Enfants, Centre Hospitalier Universitaire IBN Sina, Rabat, Maroc.
Samia El HilaliLaboratoire de Médecine Sociale, Laboratoire de Biostatistiques, Recherche Clinique et Epidémiologie, UPR de Santé Publique, Faculté de Médecine et de Pharmacie, Université Mohammed V, Rabat, Maroc.
Yassine SarbouteLaboratoire de Médecine Sociale, Laboratoire de Biostatistiques, Recherche Clinique et Epidémiologie, UPR de Santé Publique, Faculté de Médecine et de Pharmacie, Université Mohammed V, Rabat, Maroc.
Majdouline ObtelLaboratoire de Médecine Sociale, Laboratoire de Biostatistiques, Recherche Clinique et Epidémiologie, UPR de Santé Publique, Faculté de Médecine et de Pharmacie, Université Mohammed V, Rabat, Maroc.
Asmaa Mdaghri AlaouiÉquipe de Recherche sur les Anomalies Congénitales, Faculté de Médecine et de Pharmacie, Université Mohammed V, Rabat, Maroc.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Down syndrome creates complex medical needs that require multidisciplinary care. In Morocco, there is a significant scarcity of data regarding the medical coverage for these patients. This study aims to describe the medical coverage of children with trisomy 21, as well as the medical specialities involved and the costs incurred during their care pathway, with a view to identifying areas for improvement in their care, particularly in the context of the public-private partnership that is part of the process of expanding compulsory health insurance (AMO). Methods: a descriptive cross-sectional study was conducted between January 2023 and December 2024 among children followed at the dysmorphology unit of the Rabat Children's Hospital. The data were collected via standardised forms and semi-structured interviews with parents. Results: among the 118 children included (52% boys, 48% girls), the majority were aged 6-10 (31%). 58% had no medical coverage, exposing families to direct financing. The most sought-after specialities were: endocrinology/genetics (39.8%), gastroenterology (36.4%), ophthalmology (31.4%), and cardiology (29.7%). Others, such as pediatric psychiatry (0.8%) and dentistry (2.5%), remained marginal. The highest costs were for haematology (702.5 MAD/month), developmental neurology (642 MAD/month), and cardiology (413.9 MAD/month). Conclusion: in our series, only 42% of patients had medical coverage. This finding highlights the need to provide other children with Down syndrome with better access to care, smoother check-ups, and, more generally, improved medical coverage.

Indexed as

Down SyndromeInsurance CoverageInsurance, HealthChildChild, PreschoolCross-Sectional StudiesFemaleHospitals, UniversityHumansInfantMaleMoroccochildren with disabilitiesDown syndromehealthcare costshealth coverage

Identifiers

PMID42465820
PMCPMC13373016

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.