Zobrazeno 1 - 10 of 140 pro vyhledávání: '"MURCS association"'
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Akademický článek
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Akademický článek
MURCS association and anorectal malformation: Case report of a female newborn
Autor: Sofia Morão, Fernando Chaves, Daniel Virella, Fátima Alves, Rui Alves, João Pascoal
Publikováno v: Journal of Pediatric Surgery Case Reports, Vol 18, Iss C, Pp 19-23 (2017)
MURCS association is rare, first described by Duncan et al. in 1979, including Müllerian duct aplasia, renal aplasia and cervicothoracic somite dysplasia. Levitt and Peña described in 2007 a classification of syndromic anorectal malformation (ARM)
Externí odkaz: https://doaj.org/article/7bcb37f07f574b1991cb0cf448b2bcbc
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3
Presence of Cervical Vertebral Anomalies with Concomitant Non-Communicating Hydrocephalus and Multicystic Kidney in a Female Fetus: Where VACTERL-H Meets MURCS
Autor: Jan Weichert, Amrei Welp, Nadine Berg, Jann Lennard Scharf, M Gembicki, Christoph Dracopoulos
Publikováno v: Fetal and Pediatric Pathology. 41:871-880
Background Congenital multisystemic lesions with co-occurrence of non-random malformations, such as VACTERL-H or MURCS association, often pose serious threads to the newborn and still constitute an antenatal diagnostic dilemma. Case report A malforme
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bfdb203bdc9008c117f87bdc32e6423
https://doi.org/10.1080/15513815.2021.1994068
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4
Mayer-Rokitansky-Kuster-Hauser Syndrome - A Detailed Study of Nine Cases
Autor: R G Geetha, Puneet Shirbur, Amulya Reddy Bellal
Publikováno v: Journal of Evidence Based Medicine and Healthcare, Vol 7, Iss 43, Pp 2479-2484 (2020)
BACKGROUND Mayer-Rokitansky-Küster-Hauser Syndrome or MRKH Syndrome is a rare condition and is the second most common cause of primary amenorrhea, comprising of vaginal atresia (upper two thirds), rudimentary uterus, normal fallopian tubes, ovaries,
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ed8f59f6a304f912d34149faf44f541
https://doi.org/10.18410/jebmh/2020/513
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6
Long-term follow-up on MURCS (Müllerian duct, renal, cervical somite dysplasia) association and a review of the literature
Autor: Dae Gyu Kwon, Tack Lee, Sun Kim, Yeong Seok Lee, Dong Hyun Kim, Ji Eun Lee, Seun Deuk Hwang, Aram Yang
Publikováno v: Annals of Pediatric Endocrinology & Metabolism, Vol 24, Iss 3, Pp 207-211 (2019)
Annals of Pediatric Endocrinology & Metabolism
Mullerian duct aplasia-renal aplasia-cervicothoracic somite dysplasia (MURCS) association is a unique development disorder with four common types of malformations that include uterine aplasia or hypoplasia, renal ectopy or agenesis, vertebral anomali
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::810ab005923c7f5064e5bab23d6d3e96
http://e-apem.org/upload/pdf/apem-2019-24-3-207.pdf
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7
Sprengel’s Deformity With Congenital Scoliosis Successfully Treated With Combined Posterior Spinal Instrumented Fusion and Modified Woodward’s Procedure in a 14-Year-Old Patient With MURCS Association
Autor: Shahd H Almonaie, Ozair Bin Majid, Zayed S. Al-Zayed, Mohamed Alsehly
Publikováno v: Cureus
Mullerian duct aplasia-renal agenesis-cervicothoracic somite dysplasia (MURCS) association is a rare syndrome. This unique condition consists of Mullerian duct aplasia, cervicothoracic somite dysplasia, and renal aplasia, and skeletal abnormalities m
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3afd1c5a5796f6cbc5991af3fb36552c
https://doi.org/10.7759/cureus.15669
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8
Akademický článek
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9
Common pathogenesis for sirenomelia, OEIS complex, limb-body wall defect, and other malformations of caudal structures
Autor: Roger E. Stevenson
Publikováno v: American journal of medical genetics. Part AREFERENCES. 185(5)
Decades of clinical, pathological, and epidemiological study and the recent application of advanced microarray and gene sequencing technologies have led to an understanding of the causes and pathogenesis of most recognized patterns of malformation. S
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::062a44f529843e92214f1eb0675828fb
https://pubmed.ncbi.nlm.nih.gov/33522143
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10
Congenital malformations and other comorbidities in 125 women with Mayer-Rokitansky-Küster-Hauser syndrome
Autor: Witold Kędzia, Karina Kapczuk, Kinga Iwaniec, Zbigniew Friebe
Publikováno v: European Journal of Obstetrics & Gynecology and Reproductive Biology. 207:45-49
Objective To describe congenital malformations and coexisting disorders occurring in 125 Polish women with Mayer-Rokitansky-Kuster-Hauser syndrome (MRKHS). The syndrome is defined as uterovaginal aplasia in female with normal 46,XX karyotype. Study d
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef84e4c9c497c6fc3dc804f1833583ab
https://doi.org/10.1016/j.ejogrb.2016.10.014
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