Results 21 to 30 of about 10,016 (193)

Single umbilical artery: a continuous dilemma and challenge in obstetric management

Clinical and Experimental Obstetrics & Gynecology, 2021
Background: The single umbilical artery (SUA), an entity with almost unknown etiology, is still subject to discussion regarding its clinical significance, especially when it is an isolated discovery (iSUA).
Oana Sorina Tica, Andrei Adrian Tica, Doriana Cojocaru, Irina Tica, Victor Cojocaru, Vlad Iustin Tica   +5 more
doaj   +1 more source

Title: Is Mild Idiopathic Polyhydramnios Associated with an Increased Risk for an Intrauterine Fetal Demise? A Retrospective Cohort Study

International Journal of Women's Health, 2023
Megan Pagan,1 Ryan Strebeck,1 Nafisa Dajani,1 Adam Sandlin,1 Songthip Ounpraseuth,2 Nirvana Manning,1 Everett F Magann1 1Department of Obstetrics and Gynecology, University of Arkansas for the Medical Sciences, Little Rock, AR, USA; 2Department of ...
Pagan M, Strebeck R, Dajani N, Sandlin A, Ounpraseuth S, Manning N, Magann EF   +6 more
doaj  

Twin–Twin Transfusion Syndrome Presenting as Polyhydramnios in Both Fetuses Secondary to Spontaneous Microseptostomy

American Journal of Perinatology Reports, 2013
The presence of polyhydramnios and oligohydramnios is pathognomonic for twin–twin transfusion syndrome (TTTS). However, polyhydramnios of both twins can exist in TTTS in the setting of a septostomy of the dividing membrane.
David N. Hackney, Nahla Khalek, Julie Moldenhauer, Tulin Ozcan   +3 more
doaj   +1 more source

Giant Placental Chorangioma: A Rare Case Report [PDF]

Journal of Clinical and Diagnostic Research, 2016
Chorangioma is a nontrophoblastic benign vascular tumour of the placenta, arising from the primitive chorionic mesenchyme. The clinical significance is related to the size of the tumours.
Nidhi Kataria, Amarjit Singh, Preet Kamal Bedi   +2 more
doaj   +1 more source

POLYHYDRAMNIOS

The Professional Medical Journal, 2010
Polyhydramnios is though an uncommon problem but very distressing for patient. Objectives: To locate the causative factors and neonatal outcome in polyhydramnios. Design: Case series. Setting: Department of Obstetrics and Gynaecology unit 1, Lahore General Hospital, Lahore. Period: From January 2004- December 2005.
SAADIA TARIQ, SADIA CHEEMA, ADEELA AHMAD, Naela Tarique   +3 more
openaire   +2 more sources

Pathogenetic role of vitamin D deficiency and immune-inflammatory disorders in development of fetal distress in pregnant women with chronic hydramnion

Zaporožskij Medicinskij Žurnal, 2019
The role of vitamin D deficiency and immune-inflammatory disorders in the mechanisms of fetal distress development in pregnant women with chronic polyhydramnios remains unstudied.
N. A. Haistruk, A. N. Haistruk, A. V. Melnyk, L. H. Dubas, O. L. Lovkina   +4 more
doaj   +1 more source

Comparative evaluation of fetal renal artery hemodynamics in normohydramnios, idiopathic oligohydramnios and polyhydramnios in third trimester pregnancy

iRADIOLOGY, 2023
Objective To compare the renal artery (RA) flow indices (RI and PI) among normohydramnios, idiopathic oligohydramnios, and polyhydramnios and determine applicability of fetal RA Doppler indices in predicting the pregnancy outcome.
Deepak Jain, Rajesh Kumar Singh, Jyoti Jaiswal, Pranjali Mittal, Satyabhuwan Singh Netam   +4 more
doaj   +1 more source

Prenatal diagnosis of gastroschisis on ultrasonography

Apollo Medicine, 2020
Gastroschisis is an abdominal wall defect resulting from ischemia to blood vessels that supply the abdominal wall during the first trimester of pregnancy.
Reddy Ravikanth, Vaijnath P Khanapure
doaj   +1 more source

Balancing Benefits and Risks of Indomethacin in the Management of Antenatal Bartter Syndrome: A Case Report

Frontiers in Medicine, 2022
BackgroundBartter syndrome, a very rare inherited renal tubular disorder, characterized by urinary salt wastage, hypokalemia, polyuria, and metabolic alkalosis, may manifest antenatally as severe isolated polyhydramnios.
Omar Ala' Alajjuri, Mayar Essam Samaha, Ulrich Honemeyer, Ghada Mohammed, Noha A. Mousa   +4 more
doaj   +1 more source

Spectrum of Congenital Anomalies in Myhre Syndrome—Insights Into Effects Brought by Altered TGF‐β Signaling via Gain‐of‐Function Variants in SMAD4

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is a rare genetic disorder characterized by progressive multisystem involvement. Gain‐of‐function missense heterozygous variants affecting the Ile500 residue and Arg496 residue of the SMAD4 gene are implicated in this condition.
Kawmadi Gunawardena, Alessandro De Falco, Deborah Osio, Eleanor Sherlock, Emma Kivuva, Erina Sasaki, Francis H. Sansbury, Nayana Lahiri, Patricia Foley, Sahar Mansour, Shane McKee, Tazeen Ashraf, Nicola Brunetti‐Pierri, Usha Kini   +13 more
wiley   +1 more source