Wolfram综合症;《国家医学中心11月20日期刊》病例系列报告

SAR Journal of Medical Case Reports Pub Date : 2023-07-09 DOI:10.36346/sarjmcr.2023.v04i03.001

Eduardo Sagarnaga- Quezada, A. López

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引用次数: 0

摘要

Wolfram综合症是一种罕见的常染色体遗传疾病。另外，还有didimoad(尿崩症、糖尿病、视萎缩、耳聋)。它被归类为婴儿期糖尿病的一种非自身免疫性原因，其表现通常发生在早期;该疾病的其他特征是尿崩症糖尿病、视神经萎缩、神经感觉性耳聋、精神改变和其他神经退行性疾病。

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Wolfram Syndrome; Case Series Report at the “National Medical Center 20 De Noviembre ISSSTE”

Wolfram syndrome it’s a rare autosomal genetic disease. Also, kwon as DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness). Its classified as one of infancy onset diabetes mellitus non autoimmune causes, its presentation generally happens at an early age; other characteristics of the disease are insipidus diabetes, optic atrophy, neurosensorial deafness, psychiatric alterations and other neurodegenerative disorders.

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来源期刊

SAR Journal of Medical Case Reports

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