Rare association of Turner syndrome and Mayer-Rokitansky-Kuster Hauser syndrome

Amadou Ndiade; Mbaye Thiam; Sérigne A. M. Dia; Mama Sy

doi:10.18203/2320-1770.ijrcog20223141

Authors

Amadou Ndiade Laboratory of Clinical Cytology, Cytogenetics, Reproductive Biology and Human Development, Heinrich Lubke Regional Hospital of Diourbel, Senegal http://orcid.org/0000-0001-7127-0196
Mbaye Thiam Department of Radiology and Medical Imaging, Fann Hospital, Dakar, Senegal
Sérigne A. M. Dia Department of Radiology and Medical Imaging, Fann Hospital, Dakar, Senegal
Mama Sy Laboratory of Embryology and Cytogenetics Histology of the University Cheikh Anta Diop, Dakar, Senegal

DOI:

https://doi.org/10.18203/2320-1770.ijrcog20223141

Keywords:

Turner syndrome, MRKH syndrome, Senegal

Abstract

Turner syndrome and Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a rare association. The incidences of Turner and MRKH syndromes are estimated at 1/2000 and 1/4500 female births respectively. This is a 23-year-old patient, born of a consanguineous marriage, who was referred to us for exploration of primary amenorrhoea. The karyotype, performed three times, from peripheral blood lymphocytes was 45X0. The diagnosis of Turner syndrome associated with MRKH syndrome was retained.

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Author Biography

Amadou Ndiade, Laboratory of Clinical Cytology, Cytogenetics, Reproductive Biology and Human Development, Heinrich Lubke Regional Hospital of Diourbel, Senegal

formation and resaech unity in health and sustainable developement

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