Mayer-Rokitansky-Kuster-Hauser syndrome type II: A rare case

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Pai, Anand and Shakir, Mohammad (2013) Mayer-Rokitansky-Kuster-Hauser syndrome type II: A rare case. Indian Journal of Human Genetics, 19 (1). p. 113. ISSN 0971-6866

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Abstract

Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a malformation complex with absent vagina and absent or rudimentary uterus. Type II MRKH involves Mullerian duct aplasia, renal dysplasia, and cervical somite anomalies. The condition may result from early developmental disturbances in the intermediate mesoderm affecting the pronephric ducts and subsequent differentiation of Wolffian and Mullerian ducts. Few cases are reported. This paper presents a case of type II MRKH syndrome. © 2014 Elsevier B.V., All rights reserved.

Item Type: Article
Subjects: Biochemistry, Genetics and Molecular Biology > Genetics
Biochemistry, Genetics and Molecular Biology > Genetics (clinical)
Divisions: Engineering and Technology > Aarupadai Veedu Institute of Technology, Chennai, India > Physics
Depositing User: Unnamed user with email techsupport@mosys.org
Last Modified: 10 Dec 2025 06:54
URI: https://ir.vmrfdu.edu.in/id/eprint/4223

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