دورية أكاديمية

Maternally inherited diabetes mellitus and deafness (MIDD): A case report and review of literature

التفاصيل البيبلوغرافية
العنوان: Maternally inherited diabetes mellitus and deafness (MIDD): A case report and review of literature
المؤلفون: Prabhat K Agrawal, Nikhil Pursnani, Ashish Gautam, Akhil P Singh, Awadhesh K Singh
المصدر: Journal of Diabetology, Vol 14, Iss 3, Pp 173-176 (2023)
بيانات النشر: Wolters Kluwer Medknow Publications, 2023.
سنة النشر: 2023
المجموعة: LCC:Diseases of the endocrine glands. Clinical endocrinology
مصطلحات موضوعية: m.3243a>g, maternal diabetes, mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes, midd, mitochondrial diabetes, mtdna, Diseases of the endocrine glands. Clinical endocrinology, RC648-665
الوصف: Maternally inherited diabetes and deafness (MIDD) is a rare subtype of diabetes with a prevalence of up to 1% globally but often missed if not suspected. We present a case of MIDD and a thorough review of the literature related to it. The phenotypic presentation of diabetes depends on heteroplasmy levels of m.3243A>G mutation of the individual patient. Patients with MIDD may have involvement of other organs such as eye, muscles, kidney, and heart. In our patient, along with diabetes and deafness, there was also an associated vision loss with a strong maternal inheritance of diabetes. A young male who presented with diabetic ketoacidosis (DKA) and hearing and vision impairment and on further diagnostic work up turned out to be a case of genetically confirmed (m.3243A>G mutation) MIDD. To the best of our knowledge, this should be the first case of MIDD presenting as DKA being reported from India.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2078-7685
Relation: http://www.journalofdiabetology.org/article.asp?issn=2078-7685;year=2023;volume=14;issue=3;spage=173;epage=176;aulast=Agrawal; https://doaj.org/toc/2078-7685
DOI: 10.4103/jod.jod_21_23
URL الوصول: https://doaj.org/article/a0e8144bf36a4277b26145b94a5ef64a
رقم الأكسشن: edsdoj.0e8144bf36a4277b26145b94a5ef64a
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20787685
DOI:10.4103/jod.jod_21_23