"Hydrops Fetalis" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Abnormal accumulation of serous fluid in two or more fetal compartments, such as SKIN; PLEURA; PERICARDIUM; PLACENTA; PERITONEUM; AMNIOTIC FLUID. General fetal EDEMA may be of non-immunologic origin, or of immunologic origin as in the case of ERYTHROBLASTOSIS FETALIS.
- Hydrops Fetalis
- Edema, Fetal
- Fetal Edema
- Fetal Hydrops
- Hydrops, Fetal
Hydrops Fetalis, Non-Immune
- Hydrops Fetalis, Non-Immune
- Hydrops Fetalis, Nonimmune
- Hydrops Fetali, Nonimmune
- Nonimmune Hydrops Fetali
- Nonimmune Hydrops Fetalis
- Hydrops Fetalis Nonimmune
- Fetalis Nonimmune, Hydrops
- Fetalis Nonimmunes, Hydrops
- Hydrops Fetalis Nonimmunes
- Nonimmune, Hydrops Fetalis
- Nonimmunes, Hydrops Fetalis
- Idiopathic Hydrops Fetalis
- Familial Non-Immune Hydrops Fetalis
- Familial Non Immune Hydrops Fetalis
- Non-Immune Hydrops Fetalis
- Hydrops Fetalis, Idiopathic
- Fetali, Idiopathic Hydrops
- Fetalis, Idiopathic Hydrops
- Hydrops Fetali, Idiopathic
- Idiopathic Hydrops Fetali
Below are MeSH descriptors whose meaning is more general than "Hydrops Fetalis".
Below are MeSH descriptors whose meaning is more specific than "Hydrops Fetalis".
This graph shows the total number of publications written about "Hydrops Fetalis" by people in this website by year, and whether "Hydrops Fetalis" was a major or minor topic of these publications.
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Below are the most recent publications written about "Hydrops Fetalis" by people in Profiles.
Imbalances in circulating angiogenic factors in the pathophysiology of preeclampsia and related disorders. Am J Obstet Gynecol. 2022 02; 226(2S):S1019-S1034.
Recurrent Non Immune Fetal Hydrops Associated With IPEX Syndrome. Pediatr Dev Pathol. 2019 Oct; 22(5):465-471.
Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations. Eur J Med Genet. 2020 Jan; 63(1):103624.
Expanding the differential diagnosis of fetal hydrops: an unusual prenatal presentation of megalencephaly-capillary malformation syndrome. Prenat Diagn. 2013 Oct; 33(10):1010-2.
Placental origins of angiogenic dysfunction in mirror syndrome. Hypertens Pregnancy. 2012; 31(2):211-7.
Mucopolysaccharidosis type VII as a cause of recurrent non-immune hydrops fetalis. J Perinat Med. 2003; 31(6):535-7.
Twin-twin transfusion syndrome: rapid development of severe hydrops of the donor following selective feticide of the hydropic recipient. Am J Obstet Gynecol. 1993 Jul; 169(1):166-8.
Prenatal ultrasonographic diagnosis of intracranial teratoma and massive craniomegaly with associated high-output cardiac failure. Am J Obstet Gynecol. 1993 Jan; 168(1 Pt 1):97-9.
Nonimmune fetal hydrops caused by bilateral type III congenital cystic adenomatoid malformation of the lung at 17 weeks' gestation. Am J Obstet Gynecol. 1992 Aug; 167(2):503-5.
Severe fetal hydrops resulting from ABO incompatibility. Obstet Gynecol. 1991 Nov; 78(5 Pt 2):897-9.