Zobrazeno 1 - 10
of 303
pro vyhledávání: '"Mullerian anomaly"'
Publikováno v:
BMC Pregnancy and Childbirth, Vol 24, Iss 1, Pp 1-6 (2024)
Abstract Background Non-communicating rudimentary horn pregnancy (NCRHP) lead to life-threatening condition for both mother and fetus. Early diagnosis of NCRHP and laparoscopic resection is important to prevent catastrophic conditions. However, delay
Externí odkaz:
https://doaj.org/article/67de9073c05f416fb7062ff999bc2397
Publikováno v:
American Journal of Perinatology Reports, Vol 14, Iss 01, Pp e26-e30 (2024)
Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) is a rare congenital developmental syndrome manifested by uterine duplication, lower genital tract obstruction, and unilateral renal anomaly. Literature on reproductive outcomes in this pat
Externí odkaz:
https://doaj.org/article/67ca83db565848f7bad1536ea0eadee2
Akademický článek
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Akademický článek
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Autor:
Ettedal A. Aljahdali, Leena I. Sharafuddin, Wejdan O. Baamer, Maram A. Enani, Fotoon S. Alzhrani
Publikováno v:
Annals of Pediatric Surgery, Vol 18, Iss 1, Pp 1-7 (2022)
Abstract Background Müllerian anomaly is a congenital defect in the development of the female reproductive system that varies according to the stage of developmental failure resulting in agenesis, hypoplasia, or fusion defect in one or both Mulleria
Externí odkaz:
https://doaj.org/article/0fcf3b42b7354e92aa58f1966fd448bf
Publikováno v:
MGM Journal of Medical Sciences, Vol 9, Iss 1, Pp 126-129 (2022)
Uterine malformations can result from various alterations in the normal development of Mullerian ducts that make up a diverse category of congenital anomalies. In most cases, the defect remains undiagnosed and exhibits the normal number of chromosome
Externí odkaz:
https://doaj.org/article/c46016772f2345409e207aadc8cef006
Autor:
Iori Kisu, Kanako Nakamura, Tetsuro Shiraishi, Tomoko Iijima, Moito Iijima, Kiyoko Matsuda, Nobumaru Hirao
Publikováno v:
BMC Women's Health, Vol 21, Iss 1, Pp 1-6 (2021)
Abstract Background Robert’s uterus is a rare Mullerian anomaly, which can be described as an asymmetric, septate uterus with a non-communicating hemicavity. Herein, we present the case of a misdiagnosed Robert’s uterus, resulting in an invasive
Externí odkaz:
https://doaj.org/article/ae150f907be94759a08954939b0952c9
Publikováno v:
Journal of Human Reproductive Sciences, Vol 14, Iss 3, Pp 313-316 (2021)
OHVIRA syndrome comprises uterine didelphys, obstructed hemivagina, and ipsilateral renal agenesis. It usually presents with pain abdomen and pelvic or vaginal mass with normal menses. Early diagnosis is important to prevent complications in later li
Externí odkaz:
https://doaj.org/article/7ba51771957548c8a47660e19fadfc73
Autor:
Bharti Joshi, Aayushi Kaushal, Vanita Suri, Shalini Gainder, Neelam Choudhary, Sunita Jamwal, Shruti Sharma
Publikováno v:
Journal of Human Reproductive Sciences, Vol 14, Iss 4, Pp 431-435 (2021)
Background: Uterine anomalies arise if there is agenesis of one or two mullerian ducts, or absence of fusion or reabsorption of the septum between these ducts. The process may be partial or total and affect one or multiple parts of the tract. Aims: T
Externí odkaz:
https://doaj.org/article/0392be420b434541bfe255bf1050f320
Publikováno v:
Journal of Human Reproductive Sciences, Vol 13, Iss 3, Pp 235-238 (2020)
Mullerian anomalies which cause infertility in women were described by different classification systems. We report a rare case of uterine anomaly in a 16-year-old patient presented with primary amenorrhea. Her diagnostic laparoscopy findings revealed
Externí odkaz:
https://doaj.org/article/bdd753e48a64453196852e7d841f3cee