Results 71 to 80 of about 283,076 (217)
Radiology Case ReportsFetal pleural effusion is considered a rare congenital anomaly with a reported incidence of between 1:10,000 and 1:15,000 deliveries. Fetal pleural effusion may be unilateral or bilateral, primary or secondary, congenital or acquired, isolated or a ...
David M. Sherer, MD +6 more
doaj +1 more source
Prenatal Diagnosis, EarlyView.ABSTRACT Objective This study describes the role of pre‐EXIT (Ex Utero Intrapartum Treatment) fetoscopic airway evaluation in fetuses with suspected airway obstruction. Methods Single center, retrospective, observational study including fetuses with suspected airway obstruction undergoing fetoscopic airway evaluation prior to EXIT between 2013 and 2025.
Daniel Sanin‐Ramirez +6 more
wiley +1 more source
Experience of treatment of intrauterine fetal nonimmune hydrops [PDF]
, 2012 The purpose: То determine it treatment ot non-immune hydrops fetal anemia caused by viral, through the use of intrauterine, intravascular transfusions.
Потапов, Н. Н. +9 more
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Spontaneous Resolution of Mirror Syndrome following Demise of Hydropic Twin
Case Reports in Obstetrics and Gynecology, 2012 Maternal mirror syndrome is a rare consequence of fetal hydrops. By convention, delivery is recommended in pregnancies complicated by mirror syndrome due to grave fetal prognosis. We describe a case of a dichorionic, diamniotic twin gestation complicated
Kate E. Oliver +2 more
doaj +1 more source
Nonimmune hydrops fetalis due to autosomal recessive hereditary spherocytosis
Case Reports in Women's Health, 2017 Background: Hereditary spherocytosis is the most common form of inherited hemolytic anemia and is characterized by a structural defect in the RBC membrane.
Dawn M. Hannah +2 more
doaj +1 more source
Mirror Syndrome assocciated with Patau Syndrome: A Case Report [PDF]
Revista Brasileira de Ginecologia e Obstetrícia, 2018 Mirror syndrome is an unusual pathological condition in which maternal edema in pregnancy is seen in association with severe fetal and/or placental hydrops. The disease can be life-threatening for both the mother and the fetus. The pathogenesis is poorly
Ana Sofia Pais +4 more
doaj +1 more source
Prenatal Diagnosis, EarlyView.ABSTRACT Objective To evaluate postnatal medical genetic reassessment and reinterpretation of prenatal exome sequencing (pES) in liveborn children with prenatally identified structural anomalies and nondiagnostic prenatal genetic testing. Method We performed a retrospective chart review of 61 liveborn children with fetal structural anomalies who had ...
Sophie Albert +4 more
wiley +1 more source
Curating the Fetal Genome: Experience of the ClinGen Prenatal Gene Curation Expert Panel (GCEP)
Prenatal Diagnosis, EarlyView.ABSTRACT Objective Expert prenatal focused gene‐disease curation is necessary to accurately inform clinical care in the setting of rapidly expanding prenatal genomic sequencing. Methods An international Prenatal Gene Curation Expert Panel assembled and systematically reviewed genes asserted to be associated with prenatal hydrops, stillbirth, or severe ...
Stephanie N. Galloway +37 more
wiley +1 more source
Transfusión intrauterina para el tratamiento del Hidrops fetal causado por anemia: Reporte de caso y revisión de la literatura [PDF]
, 2020 OBJECTIVE Report a case of non-immune fetal hydrops caused by anemia. Also perform a review of the literature on hydrops-associated fetal anemia. METHODOLOGY We present the case of a pregnant woman of 30 years old G1P0 with pregnancy of 22 weeks.
Rojas Arias, José Luis +17 more
core +1 more source
, 1997 We investigated 6 neonates with nonimmunologic fetal hydrops admitted to Shimane Medical University Hospital between 1979 and 1996. Chromosome analysis revealed that two of these neonates (33%) had trisomy 21 (Down syndrome).
Morikawa, Shigeru +8 more
core +1 more source