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) |