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HYDROPS FETALIS, NON IMMUNE

HYDROPS FETALIS, NON IMMUNE
HYDROPS FETALIS, IDIOPATHIC
236750
OMIM = Online Mendelian Inheritance of Men
363999
P56.9, P83.2
> 500 cases reported in the literature diseases
multifactorial, excessive accumulation of fetal fluid
associated with hydrops fetalis (Stephenson 1994): idiopathic, congenital heart disease, chromosomal defects (Turner, Down syndrome), birth defects, malformations, congenital neuroblastoma, infections, metabolic disorders (Mucopolysaccharidosis I-H/IV/VII,G(M1)-Gangliosidosis type 1, Galactosialidosis, Gaucher disease type II, Glycogenosis type II, Niemann-Pick disease type C)
Laboratory findings    Hemoglobine dec (blood)
Symptoms    anemia
    early death
    edema
    heart failure, cardiac failure
    hepatomegaly (large liver)
    hydrops fetalis
    onset, fetus
    peritoneal effusions
    pleural effusions
    splenomegaly (large spleen)