Renal dysfunction in sibs with band like calcification with simplified gyration and polymicrogyria: Report of a new mutation and review of literature

被引:10
|
作者
Aggarwal, Shagun [1 ,2 ]
Bahal, Ashish [2 ,3 ]
Dalal, Ashwin [2 ]
机构
[1] Nizams Inst Med Sci, Dept Med Genet, Hyderabad 500082, Telangana, India
[2] Ctr DNA Fingerprinting & Diagnost, Div Diagnost, Hyderabad, Andhra Pradesh, India
[3] Manipal Univ, Grad Studies, Manipal, Karnataka, India
关键词
Occludin; Band like calcification with simplified gyration and polymicrogyria; Renal dysfunction; Pseudo TORCH syndrome; INTRACRANIAL CALCIFICATION; SUBEPENDYMAL CALCIFICATION; HEMORRHAGIC DESTRUCTION; INTRAUTERINE INFECTION; CONGENITAL CATARACTS; BRAIN-DEVELOPMENT; PSEUDO-TORCH; OCCLUDIN; ENCEPHALOPATHY; MALFORMATION;
D O I
10.1016/j.ejmg.2015.11.014
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Band like calcification with simplified gyration and polymicrogyria (BLC-PMG) is a distinct neuroradiological phenotype initially reported as a pseudo-TORCH syndrome and known to result from biallelic mutations in the Occludin(OCLN) gene. This is report of a family of Indian origin with two affected sibs and segregation of a homozygous novel OCLN mutation in the exon 3(NG_028291.1(OCLN_v001): c.252delC). A literature review suggests that renal dysfunction may be an unrecognized phenotypic manifestation of OCLN mutations and monitoring for the same should form part of the clinical care of these individuals. (C) 2015 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:5 / 10
页数:6
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