Results 111 to 120 of about 1,400,939 (196)

Role of imaging in Mayer-Rokitansky-Kuster-Hauser syndrome

, 2015
Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is characterized by congenital absence of the uterus and upper 2/3 rd of vagina with a normal 46, XX karyotype and normally developed secondary sexual characteristics. It affects 1:4000 women.
Anubhav Kamal, Dhaval K Thakkar, V M Kulkarni, Sanjay M Khaladkar, Rajesh Kuber   +4 more
core   +1 more source

Island Singapore Flap Vaginoplasty of Two Adult Cases of Mayer– Rokitansky–Küster–Hauser Syndrome Type I

The Annals of African Surgery, 2019
Mayer–Rokitansky–Küster–Hauser Syndrome Type I is an emotionally distressful rare condition that limits normal sexual functioning and relationships. First described in 1989 by Wee and Joseph, the neurovascular island pudendal thigh flap (Singapore flap ...
Alex Okello Wamalwa, Stanely Ominde Khainga   +1 more
doaj  

Bilateral indirect ovarian inguinal hernia in a young female with type 1 Mayer–Rokitansky–Küster–Hauser syndrome: An extremely rare clinical context

Clinical Case Reports
Key Clinical Message Incidence of bilateral inguinal hernia encompassing bilateral ovaries in adult female is very thin and concomitant association with Mayer–Rokitansky–Küster–Hauser syndrome is out of ordinary. Along with surgical management of hernia,
Sunil Bhatta, Hemant Ojha, Meraj Alam Ansari, Anuj Shrestha   +3 more
doaj   +1 more source

Mayer-Rokitansky-Küster-Hauser Syndrome or uterus and vagina agenesis in a young patient

Medisan, 2018
The case report of a patient with syndrome of Mayer-Rokitansky-Küster-Hauser or uterus and vagina agenesis, but with functioning ovaries, assisted by a multidisciplinary team in "Tamara Bunke Bider" Northern Maternal Hospital in Santiago de Cuba, whose ...
Juana Himilce Baralt Ross, Nélida Orozco Hechavarría, Eliecer Prades Hung   +2 more
doaj  

The Rokitansky-Kuster-Hauser syndrome with chromosome XO/XX mosaicism (single pelvic kidney)

, 1982
A case of Rokitansky-Kuster-Hauser syndrome and Turner syndrome association is reported. Alongside vaginal aplasia and rudimentary uterus (typical of Rokitansky-Kuster-Hauser), the patient in fact presented XX/XO type chromosome mosaicism with 20 ...
Altieri V, Caggiano S, PANICCIA, Tarcisio, Gentile M.   +3 more
core  

Colovaginoplasty in a case of mayer-rokitansky-kuster-hauser syndrome.

APSP journal of case reports, 2014
Mayer-Rokitansky-Kuster-Hauser Syndrome (MRKHS) is characterized by various abnormalities of paramesonephric duct structures; vaginal aplasia being the commonest anomaly in the spectrum. We report a 17-year-old girl; a case of MRKHS with vaginal agenesis. The cervix was present but atretic; uterus, fallopian tubes and ovaries were normal. There were no
Muhammad, Saleem, Muhammad Zafar, Iqbal, Mazher Rafee, Jam, Mushtaq, Ahmad, Bilal, Mirza   +4 more
openaire   +1 more source

Diagnosis of a variant of Mayer-Rokitansky-Kuster-Hauser syndrome: useful MRI findings

, 2011
Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome consists of vaginal aplasia associated with other müllerian duct abnormalities. Its penetrance varies, as does the involvement of other organ systems.
Elena Fruzzetti, Sabina Giusti, Daria Perini, Giusti P, Franca Fruzzetti, Giusti S, Fruzzetti E, Perini D, Fruzzetti F, Patrizia Giusti, BARTOLOZZI, CARLO, Carlo Bartolozzi   +11 more
core   +1 more source

A Case of Mayer-Rokitansky-Kuster-Hauser Syndrome Combined with Unilateral Renal Agenesis and Pelvic Cystic Mass in Child

, 1999
The Mayer-Rokitansky-Kuster-Hauser syndrome represents a spectrum of mullerian anomalies, including vaginal agenesis with or without renal anomalies, in genotypically and phenotypically normal female subjects with normal endocrine status.
한상원, 한웅규
core  

Adolescente con síndrome de Mayer-von Rokitansky-Küster-Hauser: la importancia de un manejo integral multidisciplinario An adolescent suffering from Mayer-von Rokitansky-Küster-Hauser syndrome: the importance of an integral multidisciplinary approach

Revista Colombiana de Obstetricia y Ginecología, 2006
Se presenta el caso clásico de una adolescente con diagnóstico incidental y tardío de síndrome de Mayer-von Rokitansky-Küster-Hauser y lo que consideramos aspectos fundamentales a tener en cuenta para favorecer el diagnóstico precoz y manejo de estas ...
Gabriel Barbosa, Mario Varela-Guzmán
doaj  

Posterior mediastinal Müllerian cyst in a patient with Mayer-Rokitansky-Küster-Hauser syndrome: a case report. [PDF]

J Surg Case Rep
Aleksandrov O, Patrini D, De Luca M, Moore D, Gkikas A, Jayathilaka A.   +5 more
europepmc   +1 more source