Hydrops Fetalis

"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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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.

Descriptor ID	D015160
MeSH Number(s)	C13.703.277.060.480 C15.378.295.480 C15.378.420.826.100.350 C16.300.060.480 C16.320.365.826.100.350 C20.306.480 C23.888.277.395
Concept/Terms	Hydrops 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 Immune Hydrops Fetalis Immune Hydrops Fetalis Hydrops Fetalis, Immune

Below are MeSH descriptors whose meaning is more general than "Hydrops Fetalis".

Diseases [C]
Female Urogenital Diseases and Pregnancy Complications [C13]
Pregnancy Complications [C13.703]
Fetal Diseases [C13.703.277]
Erythroblastosis, Fetal [C13.703.277.060]
Hydrops Fetalis [C13.703.277.060.480]
Hemic and Lymphatic Diseases [C15]
Hematologic Diseases [C15.378]
Erythroblastosis, Fetal [C15.378.295]
Hydrops Fetalis [C15.378.295.480]
Hemoglobinopathies [C15.378.420]
Thalassemia [C15.378.420.826]
alpha-Thalassemia [C15.378.420.826.100]
Hydrops Fetalis [C15.378.420.826.100.350]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Fetal Diseases [C16.300]
Erythroblastosis, Fetal [C16.300.060]
Hydrops Fetalis [C16.300.060.480]
Genetic Diseases, Inborn [C16.320]
Hemoglobinopathies [C16.320.365]
Thalassemia [C16.320.365.826]
alpha-Thalassemia [C16.320.365.826.100]
Hydrops Fetalis [C16.320.365.826.100.350]
Immune System Diseases [C20]
Erythroblastosis, Fetal [C20.306]
Hydrops Fetalis [C20.306.480]
Pathological Conditions, Signs and Symptoms [C23]
Signs and Symptoms [C23.888]
Edema [C23.888.277]
Hydrops Fetalis [C23.888.277.395]

Below are MeSH descriptors whose meaning is related to "Hydrops Fetalis".

Below are MeSH descriptors whose meaning is more specific than "Hydrops Fetalis".

publications

Timeline | Most Recent

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.

Bar chart showing 18 publications over 11 distinct years, with a maximum of 5 publications in 2023

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1996	1	0	1
2003	1	0	1
2013	1	0	1
2014	1	0	1
2015	0	1	1
2019	1	0	1
2020	2	0	2
2021	2	1	3
2022	1	0	1
2023	4	1	5
2024	1	0	1

Below are the most recent publications written about "Hydrops Fetalis" by people in Profiles.

Iyer NS, Mossayebi MH, Gao TJ, Haizler-Cohen L, Di Mascio D, McLaren RA, Al-Kouatly HB. Glucose-6-phosphate dehydrogenase deficiency as a cause for nonimmune hydrops fetalis and severe fetal anemia: A systematic review. Mol Genet Genomic Med. 2024 Jul; 12(7):e2491.

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Makhamreh MM, Shivashankar K, Araji S, Critchlow E, O'Brien BM, Wodoslawsky S, Berger SI, Al-Kouatly HB. RASopathies are the most common set of monogenic syndromes identified by exome sequencing for nonimmune hydrops fetalis: A systematic review and meta-analysis. Am J Med Genet A. 2024 05; 194(5):e63494.

View in: PubMed
Brewer CJ, Makhamreh MM, Shivashankar K, McLaren R, Toro M, Berger SI, Al-Kouatly HB. PIEZO1 is the most common monogenic etiology of non-immune hydrops fetalis detected by prenatal exome sequencing. Prenat Diagn. 2023 11; 43(12):1556-1566.

View in: PubMed
Critchlow E, Wodoslawsky S, Makhamreh MM, Rice SM, Turan OM, Firman B, McLaren R, Araji S, Al-Kouatly HB. Maternal outcomes of a cohort of pregnancies affected by non-immune hydrops fetalis. Int J Gynaecol Obstet. 2024 Apr; 165(1):318-327.

View in: PubMed
Biswas S, Gomez J, Horgan R, Sibai BM, Saad A, Powel JE, Al-Kouatly HB. Mirror syndrome: a systematic literature review. Am J Obstet Gynecol MFM. 2023 09; 5(9):101067.

View in: PubMed
Al-Kouatly HB, Shivashankar K, Mossayebi MH, Makhamreh M, Critchlow E, Gao Z, Fasehun LK, Alkuraya FS, Ryan EE, Hegde M, Wodoslawsky S, Hughes J, Berger SI. Diagnostic yield from prenatal exome sequencing for non-immune hydrops fetalis: A systematic review and meta-analysis. Clin Genet. 2023 05; 103(5):503-512.

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Horgan R, Critchlow E, Wodoslawsky S, Rice S, Hecht JL, Al-Kouatly HB. Placental phenotype in non-immune hydrops fetalis with negative standard workup. Ultrasound Obstet Gynecol. 2022 11; 60(5):702-703.

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Horgan R, Youssef JA, Levy AT, Berger SI, Dreux S, Brizot ML, Boutall A, Abuhamad AZ, Angarita AM, Al-Kouatly HB. Etiology and Outcome of Isolated Fetal Ascites: A Systematic Review. Obstet Gynecol. 2021 12 01; 138(6):897-904.

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Iyer NS, Gimovsky AC, Ferreira CR, Critchlow E, Al-Kouatly HB. Lysosomal storage disorders as an etiology of nonimmune hydrops fetalis: A systematic review. Clin Genet. 2021 11; 100(5):493-503.

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Al-Kouatly HB, Makhamreh MM, Rice SM, Smith K, Harman C, Quinn A, Valcarcel BN, Firman B, Liu R, Hegde M, Critchlow E, Berger SI. High diagnosis rate for nonimmune hydrops fetalis with prenatal clinical exome from the Hydrops-Yielding Diagnostic Results of Prenatal Sequencing (HYDROPS) Study. Genet Med. 2021 07; 23(7):1325-1333.

View in: PubMed

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