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Article

Incidence, genetics, and clinical phenotype of permanent neonatal diabetes mellitus in northwest Saudi Arabia.

Pediatric diabetes - 1 Sept 2012

Habeb Abdelhadi M, Al-Magamsi Mohamed S F, Eid Ihsan M, Ali Mohamed I, Hattersley Andrew T, Hussain Khalid, Ellard Sian

Abstract excerpt

BACKGROUND: Permanent neonatal diabetes mellitus (PNDM) in European population has an incidence of at least 1 in 260 000 live births and is most commonly due to mutations in KCNJ11 and ABCC8. However, data on this condition in other populations are limited. OBJECTIVE: To define the incidence, genetic aetiology, and clinical phenotype of PNDM in Al-Madinah region, northwest Saudi Arabia. METHODS: Patients with...

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Source

Identifiers

PMID: 22060631
DOI: 10.1111/j.1399-5448.2011.00828.x

Genes

ABCC8
KCNJ11
GLIS3
INS
GCK
NEUROD1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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