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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Official URL: https://doi.org/10.9734/ajpr/2021/v6i430202
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 |
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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 |