The Open Urology & Nephrology Journal

ISSN: 1874-303X ― Volume 12, 2019

Single Nucleotide Variants in A Family of Monozygotic Twins Discordant for the Phenotype Congenital Megaureter: A Genomic Analysis

Augusto C. Soares dos Santos Junior1, 2, *, Luciana B. Rodrigues4, Raony G. Corrêa Do Carmo Lisboa Cardenas1, Patricia G.P. Couto1, Luiz A. Cunha de Marco1, Eduardo A. Oliveira3, Debora M. de Miranda1, Ana C. Simoes e Silva3
1 National Institute of Science and Technology - Molecular Medicine [INCT-MM], Universidade Federal de Minas Gerais [UFMG], Minas Gerais, Brazil
2 Nephrologist at Hospital das Clínicas, Universidade Federal de Minas Gerais [HC-UFMG], Empresa Brasileira de Serviços Hospitalares [EBSERH], Minas Gerais, Brazil
3 Department of Pediatrics, Unit of Pediatric Nephrology, Interdisciplinary Laboratory of Medical Investigation, Faculty of Medicine, UFMG, Minas Gerais, Brazil
4 Department of Basic Life Sciences, Universidade Federal de Juiz de Fora, Governador Valadares, Brazil



Congenital megaureter constitutes the second most frequent cause of hydronephrosis in children. There is still much debate on what extent environmental or genetic factors are involved in the pathogenesis of congenital megaureter.


This study aimed at investigating a pair of monozygotic twins discordant for the expression of bilateral congenital megaureter using the whole exome sequencing technique.


Peripheral blood DNA was extracted and then sequenced using the whole exome technique from a pair of twins discordant for the presence of bilateral congenital refluxing unobstructed megaureter, his parents and a set of 11 non-related individuals with confirmed diagnosis of congenital megaureter. The DNA of the set of 11 non-related individuals was pooled in three groups. The monozygotic twins and their parents had DNA samples sequenced separately. Sanger validation was performed after data was filtered.


In the proband were identified 256 candidate genes, including TBX3, GATA6, DHH, LDB3, and HNF1, which are expressed in the urinary tract during the embryonic period. After Sanger validation, the SNVs found in the genes TBX3, GATA6, DHH and LDB3 were not confirmed in the proband. The SNV chr17:36104650 in the HNF1b gene was confirmed in the proband, his twin brother and the mother, however was not found in the pool of 11 non-related individuals with congenital megaureter.


Due to the possible complex causative network of genetic variations and the challenges regarding the use of the whole exome sequencing technique we could not unequivocally associate the genetic variations identified in this study with the development of the congenital megaureter.

Keywords: CAKUT, Megaureter, Whole-exome sequencing, Twins.

Article Information

Identifiers and Pagination:

Year: 2017
Volume: 10
First Page: 11
Last Page: 19
Publisher Id: TOUNJ-10-11
DOI: 10.2174/1874303X01710010011

Article History:

Received Date: 07/11/2016
Revision Received Date: 01/03/2017
Acceptance Date: 11/03/2017
Electronic publication date: 30/05/2017
Collection year: 2017

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© 2017 Soares dos Santos Junior et al.

open-access license: This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International Public License (CC-BY 4.0), a copy of which is available at: This license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

* Address correspondence to this author at the Hospital das Clínicas, Universidade Federal de Minas Gerais [UFMG], Av. Alfredo Balena, 110, Belo Horizonte, Minas Gerais, Brazil; Zip 30.130-100; Tel: +55 31-3409-9384; E-mail:

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