Assessment Genetic Mutations in Genes ACE, AGT, AGTR1, REN in Indicate Twin-to-Twin Transfusion Syndrome

Shahin A*, Reza H, Hossein A and Mohammadreza A

Pediatrics & Neonatal Biology Open Access (PNBOA)
ISSN: 2640-2726

Review Article

Assessment Genetic Mutations in Genes ACE, AGT, AGTR1, REN in Indicate Twin-to-Twin Transfusion Syndrome

Authors: Shahin A*, Reza H, Hossein A and Mohammadreza A

DOI: 10.23880/pnboa-16000136

Volume 4, Issue 1

Abstract

TTT syndrome, also known as kidney dysgenesis, is a severe and severe renal disorder characterized by abnormal kidney development before birth. Specifically, renal structures called "proximal tubules" are either not present or undeveloped in the TTT syndrome. TTT syndrome can be caused by mutations of ACE, AGT, AGTR1, and REN genes.

Keywords: TTT syndrome; Mutations of ACE, AGT, AGTR1, and REN genes

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