Evidence map›Paper›PMID 40302952›Full record

ArticlePediatric diabetes2024

Incidence, Phenotypes, and Genotypes of Neonatal Diabetes: A 16-Year Experience. The Rare Genetic Etiologies of Neonatal Diabetes Are Common in Sudan.

Samar S Hassan, Salwa A Musa, Elisa De Franco, Russel Donis Frew, Omer O Babiker, Ghassan F Mohamadsalih, Areej A Ibrahim, Samar Abu Samra, Mohamed A Abdullah

Abstract read
In one paragraph

Article in Pediatric diabetes, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Neonatal diabetes mellitus is a significant feature of COXPD-24 caused by recessive NARS2 variants.Diabetic medicine : a journal of the British Diabetic Association · 2025
    Article
  5. Neonatal diabetes mellitus around the world: Update 2024.Journal of diabetes investigation · 2024
    Review
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.

Samar S HassanDepartment of Pediatric Endocrine and Diabetes, Gaafar Ibn Auf Pediatric Tertiary Hospital, Khartoum, Sudan.ORCID 0000-0002-9741-3383
Salwa A MusaDepartment of Pediatric Endocrine and Diabetes, Gaafar Ibn Auf Pediatric Tertiary Hospital, Khartoum, Sudan.ORCID 0000-0002-0868-0915
Elisa De FrancoInstitute of Biomedical and Clinical Science, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK.ORCID 0000-0002-1437-7891
Russel Donis FrewInstitute of Biomedical and Clinical Science, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK.
Omer O BabikerSudan Childhood Diabetes Center, Khartoum, Sudan.ORCID 0000-0002-8782-3813
Ghassan F MohamadsalihDivision of Endocrine, Department of Pediatric Medicine, Sidra Hospital, Doha, Qatar.ORCID 0000-0003-0823-1682
Areej A IbrahimDivision of Pediatric Endocrine, Department of Pediatrics, Prince Mohammed Bin Abdulaziz Hospital, Madinah, Saudi Arabia.ORCID 0009-0006-0724-5950
Samar Abu SamraSudan Childhood Diabetes Center, Khartoum, Sudan.ORCID 0009-0009-2141-5444
Mohamed A AbdullahDepartment of Pediatric Endocrine and Diabetes, Gaafar Ibn Auf Pediatric Tertiary Hospital, Khartoum, Sudan.ORCID 0000-0001-7121-8216

Funding

Wellcome Trust
6 · The paper itself

Abstract

Neonatal diabetes (ND) is a rare subtype of diabetes occurring in the first 6 months of life. High incidence has been reported among populations with high rates of consanguineous marriage. However, there is paucity of reported data from sub-Saharan African countries. We report the incidence, genotype, and phenotype of ND in a large cohort from Sudan and compare these findings to regional and international data. All infants with onset of diabetes in the first 6 months of life, attending one of the only two tertiary pediatric diabetes centers in Sudan, Gaafar Ibn Auf Pediatric Tertiary Hospital and Sudan Childhood Diabetes Center, during the period of January 2006 to December 2022 were included. Medical records were reviewed for demographic and clinical information. Genetic testing was performed for 48 patients by the Exeter Genomics laboratory in the UK and for one patient by the University of Cambridge, Metabolic Research Laboratories, UK. The estimated incidence was 4.8 per 100,000 live births. Forty-nine ND patients from 45 unrelated families were identified, and a genetic diagnosis was confirmed in 37 patients (75.5%) from 33 unrelated families. Consanguinity was reported in 34 families (75.6%). The commonest genetic cause for permanent neonatal diabetes was

Indexed as

Diabetes MellitusInfant, Newborn, DiseasesConsanguinityeIF-2 KinaseFemaleGenotypeHumansIncidenceInfantInfant, NewbornMalePhenotypeRetrospective StudiesSudanEIF2AK3 protein, humaneIF-2 Kinase

Identifiers

PMID40302952
PMCPMC12016844

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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.