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359571

Atypical Mayer–Rokitansky–Kuster–Hauser syndrome − report of a rare case

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Last updated: 29 Dec 2024

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Abstract

Mayer–Rokitansky–Kuster–Hauser syndrome is a rare disorder affecting 1 in 5000 women. It is characterized by congenital absence of the uterus and the vagina in a phenotypically and karyotypically normal female. Here, we report a case of atypical Mayer–Rokitansky–Kuster–Hauser in a 13-year-old girl who also had abnormalities in the ovaries.

DOI

10.4103/kamj.kamj_11_18

Keywords

ATYPICAL, Mayer–Rokitansky–Kuster–Hauser syndrome, mullerian ageanesis

Authors

First Name

Ankita

Last Name

Dhanuka

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First Name

Anindya

Last Name

Adhikari

MiddleName

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Orcid

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First Name

Priyanka

Last Name

Agarwala

MiddleName

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Affiliation

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First Name

Palash K.

Last Name

Mandal

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Volume

24

Article Issue

3

Related Issue

48355

Issue Date

2018-09-01

Receive Date

2018-03-16

Publish Date

2018-09-01

Print ISSN

1687-4625

Online ISSN

2356-8097

Article File

KAMJ3595711535752800.pdf

PDF . 931.0kB

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https://kamj.journals.ekb.eg/article_359571.html

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https://kamj.journals.ekb.eg/service?article_code=359571

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359,571

Publication Type

Journal

Publication Title

Kasr Al Ainy Medical Journal

Publication Link

https://kamj.journals.ekb.eg/

MainTitle

Atypical Mayer–Rokitansky–Kuster–Hauser syndrome − report of a rare case

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Article

Created At

29 Dec 2024