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Quoted phrase not found in phrase index: "Mayer-Rokitansky-Kuster-Hauser syndrome type 2"
Page 1
Mayer-Rokitansky-Kuster-Hauser syndrome as an interdisciplinary problem.
Liszewska-Kapłon M, Strózik M, Kotarski Ł, Bagłaj M, Hirnle L. Liszewska-Kapłon M, et al. Adv Clin Exp Med. 2020 Apr;29(4):505-511. doi: 10.17219/acem/118850. Adv Clin Exp Med. 2020. PMID: 32348039 Free article. Review.
The Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome, also known as Mullerian agenesis or aplasia, is a congenital disease manifested by the aplasia of the uterus and the upper 2/3 of the vagina; its incidence is 1 in 4,000-5,000 female live births. We can distinguish 2 …
The Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome, also known as Mullerian agenesis or aplasia, is a congenital disease manifested by the a …
Renal abnormalities associated with Mayer-Rokitansky-Kuster-Hauser syndrome.
Dorosiev E, Muzikadzhieva G, Mladenov B, Stoev I, Velev D. Dorosiev E, et al. Folia Med (Plovdiv). 2021 Oct 31;63(5):815-818. doi: 10.3897/folmed.63.e63325. Folia Med (Plovdiv). 2021. PMID: 35851218
Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a rare congenital disorder affecting female reproductive system (agenesis of uterus and upper part of vagina) alone (type 1), or associated with abnormalities of other organs and systems (type 2). ...
Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a rare congenital disorder affecting female reproductive system (agenesis of uterus and up …
Primary Amenorrhea Due to Anatomical Abnormalities of the Reproductive Tract: Molecular Insight.
Kapczuk K, Kędzia W. Kapczuk K, et al. Int J Mol Sci. 2021 Oct 25;22(21):11495. doi: 10.3390/ijms222111495. Int J Mol Sci. 2021. PMID: 34768925 Free PMC article. Review.
Congenital anomalies of the female reproductive tract that present with primary amenorrhea involve Mullerian aplasia, also known as Mayer-Rokitansky-Kuster-Hauser syndrome (MRKHS), and cervical and vaginal anomalies that completely …
Congenital anomalies of the female reproductive tract that present with primary amenorrhea involve Mullerian aplasia, also kno …
Mayer-Rokitansky-Kuster-Hauser Syndrome: MR Manifestations Of Typical And Atypical Cases.
Khan N, Khaliq M, Azam MM, Raja R. Khan N, et al. J Ayub Med Coll Abbottabad. 2021 Oct-Dec;33(Suppl 1)(4):S711-S716. J Ayub Med Coll Abbottabad. 2021. PMID: 35077614 Free article.
MRI pelvis of the study patients was performed and evaluated by two experienced radiologists. RESULTS: The mean age of study patients was 22.2 years. Out of 19 study patients, 16 (84%) had type I while 3 (16%) had type II MRKH syndrome. ...
MRI pelvis of the study patients was performed and evaluated by two experienced radiologists. RESULTS: The mean age of study patients was 22 …
Clinical and Radiological Findings in Mayer-Rokitansky-Kuster-Hauser Syndrome Type 2: Case report.
Odhaib SA, Mohammed MJ, Al-Ali AJH, Mansour AA. Odhaib SA, et al. Sultan Qaboos Univ Med J. 2021 Nov;21(4):635-638. doi: 10.18295/squmj.4.2021.036. Epub 2021 Nov 25. Sultan Qaboos Univ Med J. 2021. PMID: 34888086 Free PMC article.
Mayer-Rokitansky-Kuster-Hauser syndrome (MRKHS) or Mullerian agenesis represents uterovaginal aplasia or hypoplasia of unknown aetiology in young women with usual 46,XX karyotype and normal secondary sexual characteristics. ...The ovaries were n …
Mayer-Rokitansky-Kuster-Hauser syndrome (MRKHS) or Mullerian agenesis represents uterovaginal aplasia or …
Typical and Atypical Associated Findings in a Group of 346 Patients with Mayer-Rokitansky-Kuester-Hauser Syndrome.
Rall K, Eisenbeis S, Henninger V, Henes M, Wallwiener D, Bonin M, Brucker S. Rall K, et al. J Pediatr Adolesc Gynecol. 2015 Oct;28(5):362-8. doi: 10.1016/j.jpag.2014.07.019. Epub 2014 Nov 11. J Pediatr Adolesc Gynecol. 2015. PMID: 26148785 Review.
A complete review of the literature was included. RESULTS: Among our cohort of 346 patients, we found that 53.2% had MRKH type 1, 41.3% had MRKH type 2, and 5.5% had MURCS syndrome. The group with associated malformations included 57.6% renal, 44.4% sk …
A complete review of the literature was included. RESULTS: Among our cohort of 346 patients, we found that 53.2% had MRKH type …
Clinical characteristics of 1,055 Chinese patients with Mayer-Rokitansky-Kuster-Hauser syndrome: a nationwide multicentric study.
Chen N, Pan H, Luo G, Wang P, Xie Z, Hua K, Luo X, Huang X, Liu Q, Sun L, Hu W, Tao G, Zhao S, Wu N, Zhu L. Chen N, et al. Fertil Steril. 2021 Aug;116(2):558-565. doi: 10.1016/j.fertnstert.2021.02.033. Epub 2021 Mar 19. Fertil Steril. 2021. PMID: 33745726 Free article.
RESULT(S): Of the 1,055 Chinese Han patients with MRKH, 69.6% had type I MRKH syndrome and the remaining 30.4% had type II MRKH syndrome. ...Skeletal malformations were the most common associated extragenital malformations in the study (22.0%, 232/1,055), of which i …
RESULT(S): Of the 1,055 Chinese Han patients with MRKH, 69.6% had type I MRKH syndrome and the remaining 30.4% had type II MRK …
Variants in genes related to development of the urinary system are associated with Mayer-Rokitansky-Kuster-Hauser syndrome.
Chu C, Li L, Li S, Zhou Q, Zheng P, Zhang YD, Duan AH, Lu D, Wu YM. Chu C, et al. Hum Genomics. 2022 Mar 31;16(1):10. doi: 10.1186/s40246-022-00385-0. Hum Genomics. 2022. PMID: 35361250 Free PMC article.
All identified variants were absent or rare in gnomAD East Asian populations. Two of the 11 variants (18.2%) were classified as pathogenic according to the ACMG guidelines, and the remaining nine (81.8%) were classified as variants of uncertain significance. Robetta online …
All identified variants were absent or rare in gnomAD East Asian populations. Two of the 11 variants (18.2%) were classified as patho …
Implications of Ehlers-Danlos Syndrome in a Patient With Mayer-Rokitansky-Kuster-Hauser Syndrome.
Brander EPA, Dietrich JE. Brander EPA, et al. J Pediatr Adolesc Gynecol. 2021 Dec;34(6):890-892. doi: 10.1016/j.jpag.2021.06.002. Epub 2021 Jun 11. J Pediatr Adolesc Gynecol. 2021. PMID: 34119661
This case report aims to describe the intersection of MRKH and EDS and its impact on vaginal dilation. CASE: A 16-year-old girl with joint hypermobility and type III EDS presented with primary amenorrhea and a karyotype of 46 XX. ...Following her diagnosis, she received va …
This case report aims to describe the intersection of MRKH and EDS and its impact on vaginal dilation. CASE: A 16-year-old girl with joint h …
Neovagina Creation: A Novel Improved Laparoscopic Vecchietti Procedure in Patients with Mayer-Rokitansky-Küster-Hauster Syndrome.
Wang YY, Duan H, Zhang XN, Wang S. Wang YY, et al. J Minim Invasive Gynecol. 2021 Jan;28(1):82-92. doi: 10.1016/j.jmig.2020.04.006. Epub 2020 Apr 10. J Minim Invasive Gynecol. 2021. PMID: 32283327
A total of 79 patients with MRKH syndrome underwent our new improved Vecchietti vaginoplasty, of whom 44 (55.7%) were diagnosed as Type I MRKH syndrome, whereas 35 (44.3%) were Type II MRKH syndrome. ...The Female Genital Self-Image Scale assessment showed a signifi …
A total of 79 patients with MRKH syndrome underwent our new improved Vecchietti vaginoplasty, of whom 44 (55.7%) were diagnosed as Type …
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