Results 81 to 90 of about 11,687 (164)
Non-immune hydrops fetalis: Clinical experience in newborn infants
Introduction. Non-immune hydrops fetalis is a condition of excessive accumulation of extravascular fluid without identifiable circulating antibody to erythrocytes membrane antigens.
Jelena Martic +5 more
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Analysis of Non-Immune Hyrops Fetalis: Evaluation of 15 Cases
OBJECTIVES: To evaluation the ultrasound characteristics, etiological factors and perinatal outcome in hydrops fetalis. STUDY DESIGN: A total of 15 hydrops fetalis presented in our perinatology unit, were studied prospectively.
Turhan Aran +2 more
doaj
Objective: We first report a case of familial hemophagocytic lymphohistiocytosis (FHL) diagnosed in utero due to third trimester hydrops fetalis.
Fang Chen, Dong-Zhi Li
doaj +1 more source
Hydrops fetalis is a severe, life-threatening fetal condition, characterized by abnormal fluid accumulation in two or more fetal compartments. This thesis focuses on both immune and non-immune hydrops fetalis (NIHF), with the emphasis on the latter due ...
Rehmann, Felicitas,
core
Lysosomal storage diseases in non-immune hydrops fetalis pregnancies.
Contains fulltext : 50653.pdf (Publisher’s version ) (Open Access)BACKGROUND: At least 20 inborn errors of metabolism may cause hydrops fetalis. Most of these are lysosomal storage diseases. The study proposes a diagnostic flowchart for
Pim M.W. Janssens +29 more
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Nonimmune hydrops fetalis associated with extralobar pulmonary sequestration: Case report
Nonimmune hydrops fetalis is a rare congenital anomaly resulting from a variety of conditions. Extralobar pulmonary sequestration leads to hydrops and hypoplasia of the adjacent structures.
core
Non-immunological hydrops fetalis [PDF]
A case of hydrops fetalis which was not due to isoimmunization is presented. The condition was diagnosed antenatally by means of Ultrasonography and the infant was delivered at 32 weeks' gestation.
Riseborough, Jennifer +2 more
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Prenatal Diagnosis of Congenital Cystic Adenomatoid Malformations: Evolution and Outcome
Objective: The aim of this study was to describe the natural history and outcomes of fetal congenital cystic adenomatoid malformation (CCAM) of the lung in three antenatally diagnosed cases.
Wei-Shiu Chen +3 more
doaj +1 more source
We report a female infant with congenital lymphedema, facial anomalies, intestinal lymphangiectasia consistent with a diagnosis of Hennekam syndrome.
BOCCARDO, FRANCESCO +8 more
core +1 more source
A 35-year-old woman presented at 27-week gestation with hypertension and pedal edema. Antenatal scan showed hydrops fetalis and growth restriction. Cordocentesis showed severe fetal anemia.
Ekta Bhutada +4 more
doaj +1 more source

