scholarly journals Partial Müllerian Duct Retention in Smad4 Conditional Mutant Male Mice

2016 ◽  
Vol 12 (6) ◽  
pp. 667-676 ◽  
Author(s):  
Fabrice G. Petit ◽  
Chuxia Deng ◽  
Soazik P. Jamin
2010 ◽  
Vol 107 (37) ◽  
pp. 16142-16147 ◽  
Author(s):  
P. S. Tanwar ◽  
L. Zhang ◽  
Y. Tanaka ◽  
M. M. Taketo ◽  
P. K. Donahoe ◽  
...  

2018 ◽  
Vol 80 (4) ◽  
pp. 557-567 ◽  
Author(s):  
Anzu YAMAMOTO ◽  
Takuya OMOTEHARA ◽  
Yuuka MIURA ◽  
Tadashi TAKADA ◽  
Naoki YONEDA ◽  
...  

Author(s):  
Dr. Vinayak A. Mali ◽  
Dr.Prashanth K.

Cysts of the epididymis are usually congenital and derived from an embryonic remnant. These cysts are due to cystic degeneration of remnants of the paramesonephric or Mullerian duct and Remnants of the mesonephric duct or Wolffian duct system. Here we report a case of bilateral Epididymal cysts in a middle aged man with a complaint of scrotal lump and infertility since 15 years. He was treated with excision of the cysts under local anaesthesia and had a marked improvement in scrotal discomfort and urgency of micturition after the treatment.


2021 ◽  
pp. 1-6
Author(s):  
Evgenia Globa ◽  
Nataliya Zelinska ◽  
Nina Siryk ◽  
Anu Bashamboo ◽  
Kenneth McElreavey

Persistent Müllerian duct syndrome (PMDS) is a rare autosomal recessive disorder characterized by the lack of regression of the derivatives of the Müllerian ducts in males. Boys with this condition usually present with unilateral or bilateral cryptorchidism, inguinal hernias, and reproductive disorders with normal male genitalia. Variants in the AMH or AMHR2 genes are responsible for the development of this syndrome. The genetic diagnosis and surgery in PMDS is challenging for both the endocrinologist and the urologist. Here, we describe the management of 2 siblings from 1 family who presented with bilateral cryptorchidism and hypospadias at birth. One child had testis located in the pelvis in the position of normal ovaries, while the other child had testis which were located in the inguinal canals (bilateral inguinal cryptorchidism). Exome sequencing revealed a compound heterozygous variant in the AMHR2 gene c.1388G>A, p.R463H and c.1412G>A p.R471H. To our knowledge, hypospadias has not been described in association with PMDS.


Pathology ◽  
2019 ◽  
Vol 51 (3) ◽  
pp. 335-336
Author(s):  
Wai Chee Lo ◽  
Kwok Leung Ng ◽  
Kam Chi Teresa Tsui ◽  
Wai Yan Candy Ng ◽  
Yuet Ping Liz Yuen

1980 ◽  
Vol 18 (2) ◽  
pp. 99-101 ◽  
Author(s):  
John A. Rock ◽  
Theodore A. Baramki ◽  
Tim H. Parmley ◽  
Howard W. Jones

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