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
core
A preterm neonate with fetal anemia and immune hydrops fetalis requiring intrauterine transfusion and postnatal exchange transfusion: a case report [PDF]
Hydrops fetalis is a presenting illness with various immune and non-immune etiologies. It involves fluid accumulation in body cavities, and symptoms specific to its underlying cause.
Mehta, Ashish +4 more
core +1 more source
A case of non-immune hydrops fetalis with maternal mirror syndrome diagnosed by trio-based exome sequencing: An autopsy case report and literature review. [PDF]
Tano S +12 more
europepmc +1 more source
Antenatal shunting and outcomes in fetuses with non-immune hydrops fetalis
Abstract Objectives Hydrops fetalis is associated with high morbidity and perinatal mortality. The aim of our study was to compare the outcomes of infants who had non-immune hydrops fetalis (NIHF) who did or did not undergo antenatal shunting .
Valentina Fragala +5 more
openaire +2 more sources
Hydrops fetalis with cystic hygroma: A case report
Hydrops fetalis is an excess accumulation of fluid in the fetus. Depending on the severity and cause of hydrops, there may be edema of fetus and placenta, ascites, pleural effusions and/or pericardial effusions.
Mohammed Khairy Ali +3 more
core +1 more source
Non-immune hydrops fetalis secondary to congenital chylothorax with diffuse interstitial lung disease: a diagnostic conundrum. [PDF]
Ngeow AJH +4 more
europepmc +1 more source
Clinical Profile and Predictors of Mortality in Neonates Born With Non-Immune Hydrops Fetalis: Experience From a Lower-Middle-Income Country. [PDF]
Hasija VK +6 more
europepmc +1 more source
Hydrops fetalis associated with erythrocyte pyruvate kinase deficiency
The authors report a case of hydrops fetalis due to severe pyruvate kinase deficiency, the most unusual clinical manifestation of this disease. Conclusion Pyruvate kinase deficiency, as other erythrocyte enzymopathies, must be considered in the ...
Costa, Elísio +8 more
core
The peroxisomal biogenesis disorders (PBDs) comprise the Zellweger spectrum disorders (i.e., Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease) and rhizomelic chondrodysplasia punctata.
Waterham, H. R. +5 more
core +1 more source
Prenatally diagnosed lethal type Larsen-like syndrome associated with bifid tongue
Larsen syndrome is characterized by multiple joint dislocations, associated with a typical facial appearance and frequently other abnormalities. Both dominant and recessive patterns of inheritance have been reported.
Diclehan Orhan +5 more
doaj

