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02 February 2016
Bryce Renwick1, Catherine Beattie2, Khurram Khan3, Raj Velu4, Donald Reid1, Donald Bain1 1) Department of Vascular Surgery, Hairmyres Hospital, Glasgow, Scotland, UK; 2) Glasgow University,

PERSISTENT MULLERIAN DUCT SYNDROME PRESENTING AS AN INGUINAL HERNIA : A CASE REPORT

Amit Dangi1, Sandhya Gupta1, Vinod Tamaknand1, Rajesh Godara1, Pradeep Garg1.

1) PGIMS Rohtak, University of Health Sciences, Haryana, India.

Disclosure: The author has declared no conflicts of interest.

Received: 24.09.15 Accepted: 10.10.15

Citation: 10.5455/ijsm.20151010105707

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Abstract:

A brief report of persistent mullerian duct syndrome (PMDS) with 46XY karyotype which is one of the rarest variety of disorders of sexual differentiation (DSD) accounting only 5% cases of all is being presented. A 21 years old male with left inguinal hernia and absent right testis presented in surgical outdoor and was operated. On exploration female genital organs like uterus and fallopian tubes along with contralateral testis were present in left inguinal canal as a content of sliding left inguinal hernia.

Keywords: Mullerian duct syndrome, karyotype, disorders of sexual differentiation (DSD), cryptorchidism, inguinal hernia.


How to Cite this Article

Bibliography

Dangi, A., Gupta, S., Tamaknand, V., Godara, R. and Garg, P. (2017) ‘Persistent Mullerian duct syndrome presenting as an inguinal hernia: A case report’, International Journal of Surgery and Medicine, , p. Online First. doi: 10.5455/ijsm.20151010105707.

Citations, Quotes & Annotations

Dangi, A., Gupta, S., Tamaknand, V., Godara, R. and Garg, P. (2017) ‘Persistent Mullerian duct syndrome presenting as an inguinal hernia: A case report’, International Journal of Surgery and Medicine, , p. Online First. doi: 10.5455/ijsm.20151010105707.
(Dangi et al., 2017)
Last modified onSunday, 12 February 2017 22:47

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