A Case Report of Familial Mayer-Rokitansky-Küster-Hauser Syndrome as Part of the Phenotypic Spectrum of the 2q37 Deletion-Reference-Cited by-同舟云学术

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A Case Report of Familial Mayer-Rokitansky-Küster-Hauser Syndrome as Part of the Phenotypic Spectrum of the 2q37 Deletion

Published:2024-02 Issue:1 Volume:37 Page:95-97
ISSN:1083-3188
Container-title:Journal of Pediatric and Adolescent Gynecology
language:en
Short-container-title:Journal of Pediatric and Adolescent Gynecology

Author:

Daum Hagit,Kremer Einav,Frumkin Ayala,Meiner Vardiella,Diamant Hagit,Harel Iris,Bauman Dvora

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology,General Medicine,Pediatrics, Perinatology and Child Health

Reference10 articles.

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

2. Typical and Atypical Associated Findings in a Group of 346 Patients with Mayer-Rokitansky-Kuester-Hauser Syndrome;Rall;J Pediatr Adolesc Gynecol,2015

3. Primary Amenorrhea Due to Anatomical Abnormalities of the Reproductive Tract: molecular Insight;Kapczuk;Int J Mol Sci,2021

4. Update on Mayer-Rokitansky-Küster-Hauser syndrome;Chen;Front Med,2022

5. Genotype and phenotype correlation in 103 individuals with 2q37 deletion syndrome reveals incomplete penetrance and supports HDAC4 as the primary genetic contributor;Le;Am J Med Genet A,2019

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: advancements and implications;Frontiers in Endocrinology;2024-04-18

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