Diabetes mellitus type 1(DM-1) in a child with usher syndrome
Department of Pediatrics, King Saud University, Riyadh, Saudi Arabia.
Research Article
World Journal of Biology Pharmacy and Health Sciences, 2023, 16(01), 229–232.
Article DOI: 10.30574/wjbphs.2023.16.1.0377
Publication history:
Received on 30 July 2023; revised on 04 September 2023; accepted on 07 September 2023
Abstract:
Usher Syndrome is a rare genetic (autosomal recessive) disorder that characterized by partial or total hearing loss caused by defective inner ear and vision loss caused by retinitis pigmentosa which worsens by time. We report on a 9 year-old child who was diagnosed by genetic testing via whole exome sequencing (WES) with Usher Syndrome. At the age of two years and three months, the patient developed type 1 Diabetes Mellitus (DM-1).
The aim of this article is to provide a comprehensive review of Usher Syndrome. The postulated association of Usher Syndrome and diabetes mellitus type 1 pathogenesis is also highlighted.
Keywords:
Diabetes Mellitus type 1; Usher Syndrome; Whole exome sequencing (WES ) association; Pathophysiolgy; Hearing; Vision; Geneti
Full text article in PDF:
Copyright information:
Copyright © 2023 Author(s) retain the copyright of this article. This article is published under the terms of the Creative Commons Attribution Liscense 4.0