A pair of siblings with Wolfram Syndrome: a review of the literature and treatment options

Wolfram syndrome (WS) is a rare genetic disorder typically characterized by juvenile onset diabetes mellitus, optic atrophy, hearing loss, diabetes insipidus, and neurodegeneration. There would be a high index of clinical suspicion for WS when clinical manifestations of type 1 diabetes and optic atr...

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Bibliographic Details
Main Authors: Png, Doanna, Yeoh, Ester, Tan, Clara, Lim, Su Chi
Other Authors: Lee Kong Chian School of Medicine (LKCMedicine)
Format: Article
Language:English
Published: 2023
Subjects:
Online Access:https://hdl.handle.net/10356/169815
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Institution: Nanyang Technological University
Language: English
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