Maternally inherited diabetes and deafness complicated by mesangial galactose-deficient IgA1 deposits: a case report

Maternally inherited diabetes and deafness complicated by mesangial galactose-deficient IgA1 deposits: a case report

Abstract Background Maternally inherited diabetes and deafness (MIDD), a mitochondrial genetic disorder, typically affects the kidneys and results in end-stage renal disease. Early diagnosis of MIDD is challenging when renal manifestations precede other key clinical features such as diabetes and dea...

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Bibliographic Details
Main Authors: Keiji Sugai, Hiroyuki Ueda, Keita Morimoto, Mai Tanaka, Daisuke Takahashi, Akio Nakashima, Junichiro Kato, Hiroshi Takahashi, Yutaka Yamaguchi, Tetsuya Kawamura, Kazushige Hanaoka, Yoichi Miyazaki, Takashi Yokoo
Format: Article
Language:English
Published: BMC 2018-12-01
Series:BMC Nephrology
Subjects:
Maternally inherited diabetes and deafness
IgA deposits
Kidney disease
Case report
Galactose-deficient IgA1 variant
Online Access:http://link.springer.com/article/10.1186/s12882-018-1152-6

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http://link.springer.com/article/10.1186/s12882-018-1152-6

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