Results 91 to 100 of about 1,143,195 (179)
Interpretative phenomenological analysis and genetic counseling
Abstract The role of qualitative methods in healthcare research has gained acceptance over the last 30 years, and there are now a number of well‐established approaches available offering a diversity of aims, procedures, and epistemological emphases. This paper focuses on one such approach, Interpretative Phenomenological Analysis (IPA), to provide a ...
Rachel A. Starr, Jonathan A. Smith
wiley +1 more source
CASE REPORT Leiomyoma Arising from Mullerian Remnant, Mimicking Ovarian Tumor in a Woman with MRKH Syndrome and Unilateral Renal Agenesis [PDF]
BACKGROUND: Leiomyoma with secondary changes arising from Mullerian remnant may mimic ovarian tumor in women with Mayer-Rockitansky-Kuster-Hauser (MRKH) syndrome in patients with pelvic mass and urologic abnormalities.
Woldeyes, W, Girma, W
core +1 more source
Attitudes toward uterus transplantation. An option for motherhood?
Despite the demonstrated feasibility of uterus transplantation as a treatment for absolute uterine infertility little is known about the acceptance of it among the target population. This study indicates that uterus transplantation is accepted by most women who would benefit from the procedure and their relatives, and also by those women who do not ...
Mariona Rius +7 more
wiley +1 more source
International Journal of Gynecology &Obstetrics, Volume 172, Issue 3, Page 1794-1795, March 2026.
Jana Moravcova +3 more
wiley +1 more source
Introduction: Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a congenital malformation of the Müllerian ducts that results in aplasia or severe hypoplasia of the upper vagina, uterus, and fallopian tubes.
Margarida Gonçalves +4 more
doaj +1 more source
A Case of Mayer–Rokitansky–Küster–Hauser Syndrome with a Fused Pancake-shaped Pelvic Kidney
Mayer–Rokitansky–Küster–Hauser (MRKH) Syndrome is a female reproductive system disorder. It is characterized by a defect in the Müllerian ducts development, and it causes the absence of the uterus in variable degrees in upper vaginal hypoplasia.
Ali Reza Eftekhari Moghadam +5 more
doaj +1 more source
Clinical Case Reports, Volume 14, Issue 2, February 2026.
Shahzeen Irshad +5 more
wiley +1 more source
MRKH syndrome and Turner syndrome co-existing in a patient with primary amenorrhoea
Mayer-Rokitansky-Haüser-Kuster (MRHK) or Mullerian agenesis syndrome is characterized by aplasia or hypoplasia of uterus and upper 2/3 of the vagina. Patients usually have normal gonadal function as both ovaries develop from different embryonic sources.
openaire +3 more sources
CTU, MRI and MRU images (DICOM format) of a MRKH syndrome patient with rare findings of inferior crossed-fused renal ectopia and Gartner's duct ...
Zhang, J (via Mendeley Data)
core +1 more source
Women with Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome do not have proper performance and sexual satisfaction because of physical problems. MRKH syndrome leads to psychological and identity problems and has a negative effect on self-concept.
Majid Mahmoud Alilou +4 more
doaj +1 more source

