Results 71 to 80 of about 26,761 (285)

Ultrasound diagnosis of hydrops fetalis in consanguineous parents

open access: yesPAMJ Clinical Medicine, 2020
This is a 25-year-old patient who has been married for 1 year to a first cousin. She is nulliparous and was pregnant with a first pregnancy at 27 weeks of gestation.
Ibrahima Niang, Mamadou Ly
doaj   +1 more source

Prenatal Sonographic Features of Fetuses in Trisomy 13 Pregnancies (III) [PDF]

open access: yes, 2009
SummaryPrenatal ultrasound is a powerful tool for the detection of structural abnormalities of fetuses in trisomy 13 pregnancies. This article provides a comprehensive review of the prenatal sonographic features of trisomy 13 fetuses in the second and ...
Al-Kouatly   +98 more
core   +2 more sources

Hydrops fetalis associated with chorioangioma and thrombosis of umbilical vein

open access: yesThe Turkish Journal of Pediatrics, 2009
Placental chorioangioma and thrombosis of an umbilical vein varix are rare etiologic factors of non-immune hydrops fetalis. Herein, we report a patient who had hydrops fetalis associated with placental chorioangioma and thrombosis of an umbilical ...
Ercan Sivasli   +6 more
doaj  

Alpha-thalassaemic hydrops fetalis. [PDF]

open access: yesArchives of Disease in Childhood, 1981
Concentrations of total protein, albumin, colloid osmotic pressure, and immunoglobulins G and M were measured in the umbilical venous plasma of 4 infants with alpha-thalassaemic hydrops fetalis. Total protein, albumin, and colloid osmotic pressure concentrations were low, and these are likely to contributory factors in the formation of fetal oedema ...
B Chaimongkol, E M Bryan, D A Harris
openaire   +2 more sources

hCALCRL mutation causes autosomal recessive nonimmune hydrops fetalis with lymphatic dysplasia

open access: yesJournal of Experimental Medicine, 2018
We report the first case of nonimmune hydrops fetalis (NIHF) associated with a recessive, in-frame deletion of V205 in the G protein–coupled receptor, Calcitonin Receptor-Like Receptor (hCALCRL). Homozygosity results in fetal demise from hydrops fetalis,
D. Mackie   +11 more
semanticscholar   +1 more source

Non-immune hydrops fetalis: etiology, pathogenesis, features of diagnosis and treatment in the fetus and newborn

open access: yesДетские инфекции (Москва)
Non-immune hydrops fetalis is a polyetiological disease characterized by high perinatal mortality. The development of non-immune fetal hydrops is associated with diseases of the cardiovascular and lymphatic systems, genetic and chromosomal diseases ...
S. V. Dumova   +8 more
doaj   +1 more source

Hydrops fetalis: Incidence, Etiologies, Management Strategies, and Outcomes

open access: yesResearch and Reports in Neonatology, 2023
Tamiko Younge,1 Katherine M Ottolini,1 Huda B Al-Kouatly,2 Seth I Berger3 1Division of Neonatology, Children’s National Hospital, Washington, DC, USA; 2Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Sidney Kimmel Medical ...
Younge T   +3 more
doaj  

Human parvovirus B19 infection and hydrops fetalis in Rio de Janeiro, Brazil

open access: yesMemorias do Instituto Oswaldo Cruz, 1996
Formalin-fixed paraffin embedded lung and liver tissue from 23 cases of non immune hydrops fetalis and five control cases, in which hydrops were due to syphilis (3) and genetic causes (2), were examined for the presence of human parvovirus B19 by DNA ...
Rita CN Cubel   +7 more
doaj   +1 more source

Pathophysiology of hydrops fetalis

open access: yesSeminars in Perinatology, 1995
Hydrops fetalis occurs when the rate of interstitial fluid production by capillary ultrafiltration exceeds the rate of interstitial fluid return to the circulation via lymphatic vessels. Developmental differences in the microcirculation and lymphatic system of the fetus, as compared with mature subjects, renders the fetus susceptible to interstitial ...
openaire   +3 more sources

Idiopathic Infantile arterial calcification –A Very rare case [PDF]

open access: yes, 2010
A rare case of Idiopathic Arterial Calcification of Infancy (IACI), inherited as an autosomal recessive disease, is ...
Joshi, PS, Sarmila, N, Vani, R
core  

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