Long-Term Evolution of Patients with the Wolcott Rallison Syndrome: Case Series of 4 Patients and Review of Literatures

Hafidi, Najlae El and Imane, Zineb (2021) Long-Term Evolution of Patients with the Wolcott Rallison Syndrome: Case Series of 4 Patients and Review of Literatures. Asian Journal of Pediatric Research, 6 (4). pp. 22-28. ISSN 2582-2950

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Abstract

Introduction: Wolcott-Rallison syndrome is a rare autosomal recessive disorder characterized by neonatal diabetes in consanguineous families. associated with liver dysfunction, epiphyseal dysplasia, and. growth retardation. It is caused by mutations in the gene encoding eukaryotic translation initiation factor 2α kinase 3 (EIF2AK3).

We report a long-term evolution of 4 patients with Wolcott Rallison syndrome.

Item Type: Article
Subjects: Open Archive Press > Medical Science
Depositing User: Unnamed user with email support@openarchivepress.com
Date Deposited: 20 Feb 2023 07:14
Last Modified: 19 Jul 2024 07:02
URI: http://library.2pressrelease.co.in/id/eprint/324

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