Zobrazeno 1 - 10
of 149
pro vyhledávání: '"FETAL MEGACYSTIS"'
Autor:
Chih-Ping Chen
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 63, Iss 1, Pp 19-21 (2024)
Fetal megacystis has been reported to be associated with chromosomal abnormalities, megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS), obstructive uropathy, prune belly syndrome, cloacal anomalies, limb-body wall complex, amniotic ban
Externí odkaz:
https://doaj.org/article/681dbecfa326466ca156dcaf0de70ac9
Autor:
Ugo Maria Pierucci, Irene Paraboschi, Guglielmo Mantica, Sara Costanzo, Angela Riccio, Giorgio Giuseppe Orlando Selvaggio, Gloria Pelizzo
Publikováno v:
Diagnostics, Vol 14, Iss 7, p 756 (2024)
Introduction: To evaluate the clinical usefulness of demographic data, fetal imaging findings and urinary analytes were used for predicting poor postnatal renal function in children with congenital megacystis. Materials and methods: A systematic revi
Externí odkaz:
https://doaj.org/article/2e49a221e1a7461abc25df54e8138af7
Autor:
Chih-Ping Chen
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 63, Iss 1, Pp 17-18 (2024)
Fetal megacystis has been reported to be associated with chromosomal abnormalities, megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS), obstructive uropathy, prune belly syndrome, cloacal anomalies, limb-body wall complex, amniotic ban
Externí odkaz:
https://doaj.org/article/103c61eb2d8b4863ac0506f3180723e9
Akademický článek
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Autor:
Roland Axt-Fliedner, Corinna Keil, Lara Sommer, Stefanie Weber, Siegmund Köhler, Martin Koemhoff, Ivonne Bedei
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 35:8536-8543
Fetal megacystis (MC) can be severe and is mainly caused by fetal lower urinary tract obstruction (LUTO). Mortality of fetal LUTO can be high as a result of pulmonary hypoplasia and/or (chronic) renal insufficiency. Several technical procedures for v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f76c8b1a51be14d007c76b9fcd7189fa
https://doi.org/10.1080/14767058.2021.1988562
https://doi.org/10.1080/14767058.2021.1988562
Publikováno v:
Fetal and Pediatric Pathology. 41:818-822
Introduction A case of spontaneous fetal bladder rupture occurring in a woman with SARS-CoV-2 pneumonia receiving invasive ventilatory support is reported. Case A 33-year-old woman was admitted at 30.6 weeks' gestation with the diagnosis of severe pn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4909ac88135848b855a87bcbcfb75932
https://doi.org/10.1080/15513815.2021.1963359
https://doi.org/10.1080/15513815.2021.1963359
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Dilek Sahin, Busra Kanyildiz, Aykan Yucel, Gokcen Orgul, Gökhan Karakoç, Hasan Eroğlu, Kemal Sarsmaz
Publikováno v:
Gynecology Obstetrics & Reproductive Medicine. :1-5
Objectives: Fetal megacystis is very rare; however this problem may be associated with other structural or chromosomal abnormalities leading to morbidity and mortality. Due to renal injury and pulmonary hypoplasia, prognosis is poor especially in fet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44978705322bf1ec75e2a323af85d9b9
https://doi.org/10.21613/gorm.2019.971
https://doi.org/10.21613/gorm.2019.971
Publikováno v:
Prenatal Diagnosis. 41:308-315
OBJECTIVES To evaluate aneuploidy rate, prognostic factors, and perinatal outcomes following a diagnosis of fetal megacystis at 11-14 week's gestation. METHODS A retrospective study of first trimester fetal megacystis from 2010 to 2020 was performed,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15ef4e086402e9ccbf66a57b09307308
https://doi.org/10.1002/pd.5868
https://doi.org/10.1002/pd.5868
Autor:
Cécile Masson, Arnaud Molin, Clarisse Billon, Agnès Liard, Lucile Boutaud, Sabine Sigaudy, Sophie Thomas, Eglantine Magnin, Radia Fritih, Valérie Layet, Maryse Bonnière, Yves Ville, Alix Clemenson, Alain Diguet, Philippe Roth, Coralie Dauge, Sophie Patrier, John Rendu, Julia Tantau, Bettina Bessières, Alice Goldenberg, Leila Hakkakian, Céline Poirsier, Tania Attié-Bitach, Ferechté Razavi, Clémence Fleury, Eric Verspyck, Nadia Elkhartoufi, Maude Grelet, Amale Achaiaa, Fabienne Prieur, Christine Bole-Feysot, Aude Tessier
Publikováno v:
Clinical Genetics. 98:261-273
Megacystis-microcolon-intestinal-hypoperistalsis syndrome (MMIHS) is a severe congenital visceral myopathy characterized by an abdominal distension due to a large non-obstructed urinary bladder, a microcolon and intestinal hypo- or aperistalsis. Most
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b785fb90b76ae17b0c8d7bcf43e09a93
https://doi.org/10.1111/cge.13801
https://doi.org/10.1111/cge.13801