Rare variant of atypical Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome with breast malformation: case report and review of literature-Reference-Cited by-同舟云学术

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Rare variant of atypical Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome with breast malformation: case report and review of literature

Published:2022-02-13 Issue:3 Volume:31 Page:141-144
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:

Author:

Mahey Reeta,Ramaswamy Anjali,Cheluvaraju Rohitha,Manchanda Smita,Bhatla Neerja

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology and Child Health

Reference14 articles.

1. Vaginal uterine agenesis associated with amastia in a phenotypic female with a de novo 46,XX,t(8;13)(q22.1;q32.1) translocation.;Amesse;Clin Genet,1999

2. Mayer-Rokitansky-Kuster-Hauser syndrome: diagnosis with MR imaging.;Hall-Craggs;Radiology,2013

3. Hyperandrogenemia and ovarian reserve in patients with Mayer-Rokitansky-Küster-Hauser syndrome type 1 and 2: potential influences on ovarian stimulation.;Henes;Arch Gynecol Obstet,2018

4. Prevalence and patient characteristics of Mayer–Rokitansky–Küster–Hauser syndrome: a nationwide registry-based study.;Herlin;Hum Reprod,2016

5. Whole-exome sequencing identifies a GREB1L variant in a three-generation family with Müllerian and renal agenesis: a novel candidate gene in Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome. A case report.;Herlin;Hum Reprod,2019

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