Focal segmental glomerulosclerosis associated with maternally inherited diabetes and deafness: Clinical pathological analysis

التفاصيل البيبلوغرافية
العنوان:	Focal segmental glomerulosclerosis associated with maternally inherited diabetes and deafness: Clinical pathological analysis
المؤلفون:	Xue-Ying Cao, Ri-Bao Wei, Yuan-Da Wang, Xue-Guang Zhang, Li Tang, Xiang-Mei Chen
المصدر:	Indian Journal of Pathology and Microbiology, Vol 56, Iss 3, Pp 272-275 (2013)
بيانات النشر:	Wolters Kluwer Medknow Publications, 2013.
سنة النشر:	2013
المجموعة:	LCC:Pathology LCC:Microbiology
مصطلحات موضوعية:	Clinical pathology, focal segmental glomerulosclerosis, maternally inherited diabetes and deafness, Pathology, RB1-214, Microbiology, QR1-502
الوصف:	Maternally inherited diabetes and deafness (MIDD), which is caused by an A to G substitution at position 3243 (m.3243A>G) in the transfer ribonucleic acid leucine gene, is characterized by diabetes and hearing loss. Patients with MIDD frequently have renal disease, which may precede the diagnosis of either diabetes or deafness or may be the sole manifestation of the m.3243A>G mutation. Recently, progressive renal failure was reported in adults, and a number of childhood cases of focal segmental glomerulosclerosis (FSGS) of MIDD have been reported. However, little is known about the glomerular lesions in FSGS in MIDD. In the present study, we reported two cases of FSGS associated with MIDD and studied the clinical features of the proband and her mother.
نوع الوثيقة:	article
وصف الملف:	electronic resource
اللغة:	English
تدمد:	0377-4929
Relation:	http://www.ijpmonline.org/article.asp?issn=0377-4929;year=2013;volume=56;issue=3;spage=272;epage=275;aulast=Cao; https://doaj.org/toc/0377-4929
DOI:	10.4103/0377-4929.120392
URL الوصول:	https://doaj.org/article/3371ff7addb44109a00f3b59e2136467
رقم الانضمام:	edsdoj.3371ff7addb44109a00f3b59e2136467
قاعدة البيانات:	Directory of Open Access Journals

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الوصف
تدمد:	03774929
DOI:	10.4103/0377-4929.120392