Results 71 to 80 of about 27,264 (283)
Radiology and Oncology, 2014 Background. Mediastinal fetal teratoma can be detected as a mass in the chest during a routine prenatal ultrasound screening. Because of the pressure on mediastinal structures it can be the cause of non-immune hydrops fetalis and polyhydramnion.
Simoncic Milanka +6 more
doaj +1 more source
Antenatal diagnosis and management of cystic hygroma with hydrops fetalis
MGM Journal of Medical Sciences, 2021 Cystic hygroma is a congenital thin-walled cyst that contains lymphatic fluids. Ultrasonography has helped in detecting more and more cases of cystic hygroma with fetal hydrops.
Saloni Pugalia +2 more
doaj +1 more source
Prenatal Diagnosis, EarlyView.ABSTRACT In utero interventions are transformative in addressing genetic and anatomic conditions during fetal development. Next generation sequencing enables early genetic testing, playing a pivotal role in prenatal decision‐making by supporting risk stratification, precise and timely diagnosis, which directly informs eligibility for fetal surgical and
Matthew A. Shear +7 more
wiley +1 more source
Nonimmune Hydrops Fetalis and Early Skeletal Changes in Congenital Syphilis: Case Series and Review of Literature [PDF]
Pediatric Infectious DiseaseAim and background: Syphilis remains the most common congenital infection in the world. During pregnancy, syphilis is associated with numerous findings, including placentomegaly, hepatomegaly, polyhydramnios, fetal nonimmune hemolytic anemia, and hydrops
Kruti N Shah +2 more
doaj +1 more source
Thai Journal of Obstetrics and Gynaecology, 2020 Non-immune hydrops (NIH) is an important condition in health service. Many etiologies of NIH have been described, but the definite cause of NIH in many cases is still reported as “unknown”. This finding may be partly explained by the inadequate
Patou Tantbirojn
doaj +1 more source
Idiopathic Infantile arterial calcification –A Very rare case [PDF]
, 2010 A rare case of Idiopathic Arterial Calcification of Infancy (IACI), inherited as an autosomal recessive disease, is ...
Joshi, PS, Sarmila, N, Vani, R
core
A system‐based approach to the genetic etiologies of non‐immune hydrops fetalis
Prenatal Diagnosis, 2019 A wide spectrum of genetic causes may lead to nonimmune hydrops fetalis (NIHF), and a thorough phenotypic and genetic evaluation are essential to determine the underlying etiology, optimally manage these pregnancies, and inform discussions about ...
Anne H Mardy +3 more
semanticscholar +1 more source
Prenatal Diagnosis, EarlyView.ABSTRACT Hemolytic disease of the fetus and newborn (HDFN) remains a significant concern in prenatal care primarily caused by maternal alloimmunization against fetal red blood cell antigens, most commonly the D antigen. Noninvasive fetal RHD genotyping, used as a screening tool, enables targeted antenatal prophylaxis and has been implemented in several
Emilie Thorup +4 more
wiley +1 more source
Cop1 constitutively regulates c-Jun protein stability and functions as a tumor suppressor in mice [PDF]
, 2011 Biochemical studies have suggested conflicting roles for the E3 ubiquitin ligase constitutive photomorphogenesis protein 1 (Cop 1; also known as Rfwd2) in tumorigenesis, providing evidence for both the oncoprotein c-Jun and the tumor suppressor p53 as ...
Aleksandra Zwolinska +43 more
core +2 more sources
Prenatal Diagnosis, EarlyView.ABSTRACT Objective To evaluate the diagnostic value of prenatal exome sequencing (ES) integrated with copy number variant (CNV) and single nucleotide variant (SNV) analysis (ES‐CNV/SNV) in fetuses with structural anomalies following negative chromosomal microarray analysis (CMA) and karyotyping, and to delineate the practical challenges encountered ...
Yulin Jiang +21 more
wiley +1 more source