Results 111 to 120 of about 2,520 (182)

Development of the human bladder and ureterovesical junction. [PDF]

, 2018
The urinary bladder collects urine from the kidneys and stores it until the appropriate moment for voiding. The trigone and ureterovesical junctions are key to bladder function, by allowing one-way passage of urine into the bladder without obstruction ...
Baskin, Laurence, Cao, Mei, Cunha, Gerald R, Liaw, Aron, Liu, Ge, Shen, Joel, Sinclair, Adriane   +6 more
core   +1 more source

Müllerian Agenesis Masquerading as Secondary Amenorrhea

Case Reports in Pediatrics, 2018
The most common cause of primary amenorrhea is congenital malformation of the Müllerian ducts, including Müllerian agenesis, also known as Mayer–Rokitansky–Küster–Hauser syndrome (MRKH).
Gloria Tavera, Rina Lazebnik
doaj   +1 more source

SMAD2/3 signaling regulates initiation of mouse Wolffian ducts and proximal differentiation in Müllerian ducts

FEBS Open Bio
Male and female reproductive tracts develop from anterior intermediate mesoderm with similar differentiation processes. The anterior intermediate mesoderm develops into the mesonephros, and the Wolffian duct initiates by epithelialization in the ...
Tadaaki Nakajima, Akihiro Imai, Chihiro Ishii, Kota Tsuruyama, Risa Yamanaka, Yasuhiro Tomooka, Shinta Saito, Noritaka Adachi, Satomi Kohno, Tomomi Sato   +9 more
doaj   +1 more source

Herlyn-Werner-Wunderlich Syndrome with Degenerating Fibroid– Uncommon Presentation of a Rare Anomaly [PDF]

Journal of Krishna Institute of Medical Sciences University, 2018
Herlyn-Werner-Wunderlich Syndrome (HWWS) is a rare congenital anomaly of Mullerian and mesonephric ducts characterized by uterus didelphys with obstructed hemivagina and ipsilateral renal agenesis.
Kanakaraj Kannan, N Pavan Kumar, Venkatraman Indiran, T Ramachandra Prasad, Prabakaran Maduraimuthu   +4 more
doaj  

Müllerian Anomalies: Revisited

Journal of Gastrointestinal and Abdominal Radiology
The Müllerian structures are developed from paired embryologic ducts that undergo fusion and resorption in utero to form the uterus, fallopian tubes, cervix, and upper two-thirds of the vagina.
Tulika Singh, Gopika Sri, Veenu Singla, Vanita Jain   +3 more
doaj   +1 more source

Persistent Mullerian Duct Syndrome [PDF]

, 2020
Ahmed H. Al-Salem, Moustafa Hamchou
openaire   +2 more sources

HYSTEROSALPINGOGRAPHY: TECHNIQUE AND APPLICATIONS (VIEW) [PDF]

, 2015
Hysterosalpingography (HSG) is the radiographic evaluation of the uterine cavity and fallopian tubes after the administration of a radio-opaque medium through the cervical canal.
Bakun, O.V., Kamal Preet, Kaur, Megha, Mittal, Neha, Kumari, Priya, Patel   +4 more
core  

Clinical aspects of Mayer-Rokitansky-Kuester-Hauser syndrome: recommendations for clinical diagnosis and staging [PDF]

, 2017
BACKGROUND: The Mayer-Rokitansky-Kuester-Hauser (MRKH) syndrome is a malformation of the female genitals (occurring in one in 4000 female live births) as a result of interrupted embryonic development of the Müllerian (paramesonephric) ducts.
Beckmann, Matthias W., Brucker, Sara, Hauser, Georges A., Kellermann, Anja, Ludwig, Kurt S., Oppelt, Peter, Renner, Stefan P., Strick, Reiner, Strissel, Pamela L., Wallwiener, Diethelm   +9 more
core  

Paraurethral cyst. A case report

Medisur, 2011
The paraurethral or Skene’s duct cyst, is a rare diagnostic entity in a newborn. It represents less than 0,5 % of congenital malformations of the urinary tract. All over the world it is reported an incidence of 1:2000 to 1:7000 in female births.
Emilio Vega Azcúe
doaj   +2 more sources

Mullerian Duct [PDF]

, 2020
openaire   +1 more source