Results 81 to 90 of about 283,076 (217)

Innovative Fetal Therapy for a Giant Congenital Pulmonary Airway Malformation with Hydrops

, 2022
Introduction: Congenital pulmonary airway malformations (CPAMs) complicated by hydrops portend significant morbidity and mortality, with fetal survival estimates less than 10%.
Klinkner, Denise B., Stenzel, Ellen Bendel, Ruano, Rodrigo, Teles Abrao Trad, Ayssa, Callstrom, Matthew R. R., Atwell, Thomas, Schenone, Mauro, Qureshi, Mohamed Yasir   +7 more
core   +1 more source

Fetal myocarditis – a precursor of undesirable consequences of intrauterine infection with parvovirus B19

Patologìâ, 2019
Objective: to conduct a retrospective analysis of the results of sonographic, virological and morphological studies of cases of non-immune hydrops fetalis followed by intrauterine fetal death because of severe cardiovascular insufficiency (SCI) against ...
N. P. Bondarenko, V. M. Zhezhera, A. V. Aksonova   +2 more
doaj   +1 more source

Spectrum of Congenital Malformations in Sex Chromosome Tetrasomies and Pentasomies: A Systematic Review

Andrology, EarlyView.
ABSTRACT Sex chromosome aneuploidies represent a heterogeneous group of chromosomal conditions, in which phenotypic complexity generally increases with the number of supernumerary sex chromosomes. While Turner syndrome and sex chromosome trisomies are relatively well characterized, less is known about congenital malformations in sex chromosome ...
Anna Colding, Jannie Traberg, Inger Lily Hjuler Dorf, Anne Skakkebæk   +3 more
wiley   +1 more source

Digoxina. A droga de escolha para o tratamento in utero da taquicardia paroxística supraventricular.

Acta Médica Portuguesa, 1997
Fetal tachyarrhythmia may constitute a risk for the fetus, therefore early treatment is indicate for all cases of tachydysrhythmia, with or without hydrops, in order to prevent irreversible hydrops.
I S Silva, C Nunes, G Mimoso, E Castela, J Mesquita   +4 more
doaj   +1 more source

Genetic Testing Unveils a Novel Thrombospondin‐1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79‐Year‐Old Woman

Clinical Genetics, EarlyView.
A 79‐year‐old woman with lifelong peripheral edema and an affected sister was found to harbor a novel homozygous THSD1 splice‐site variant. Reduced THSD1 expression in dermal endothelial cells supported the possibility that this variant contributes to chronic hereditary edema.
Eiko Amo, Takafumi Toyohara, Naoya Saijo, Satoko Sato, Jun Takayama, Yoshiko Suto, Yuji Noguchi, Sosuke Kinomura, Yusuke Ishizuka, Shun Watanabe, Koichi Kikuchi, Rui Makino, Mai Yoshida, Yuji Oe, Tasuku Nagasawa, Koji Okamoto, Takehiro Suzuki, Mariko Miyazaki, Shinya Kawaguchi, Takashi Suzuki, Takaaki Abe, Shigeo Kure, Atsuo Kikuchi, Tetsuhiro Tanaka   +23 more
wiley   +1 more source

Hidrops fetal no inmune por anemia diseritropoyética congénita

Revista Chilena de Obstetricia y Ginecología, 2011
La anemia diseritropoyética congénita se engloba dentro de un grupo raro y heterogéneo de trastornos eritrocitarios caracterizados por eritropoyesis ineficaz, anemia megaloblástica, hemosiderosis secundaria e hidrops fetal. Presentamos el caso de un feto
Laura Blasco G, Blanca Paredes R, Roberto Rodríguez G, Mar Muñoz M, Lucía Deiros B   +4 more
doaj  

Management of Congenital Complete Atrioventricular Block in Preterm Neonates With Novel Pacing Method

Pacing and Clinical Electrophysiology, EarlyView.
ABSTRACT Congenital complete atrioventricular block (CCAVB) is a rare autoimmune mediated disorder with a guarded prognosis, particularly when associated with extreme prematurity and severe bradycardia. Recent advances in neonatal care for extremely premature infants with delivery at level IV neonatal intensive care unit and novel pediatric pacing ...
Anusha Bai Kalithkar, Rodrigo Ruano, Leonardo Mulinari, Steven Fishberger, Sethuraman Swaminathan, Ileana Torres‐Burgos   +5 more
wiley   +1 more source

Impact of Managing Presumptive Fetal Membrane Hydrops in a Mare on Fetal Livability

, 2023
A case of presumptive allantois or amniotic hydrops of the fetal membranes was diagnosed in a young Intracytoplasmic Sperm Injection (ICSI) derived embryo recipient. Hydrops is a rare condition and treatment is usually focused on saving the mare.
Çağla Aytaş, Cantile, Carlo, Micaela Sgorbini, Fanelli, Diana, Rebecca Moroni, Diana Fanelli, Aytaş, Çağla, Panzani, Duccio, Bocci, Carlotta, Duccio Panzani, Sgorbini, Micaela, Irene Nocera, Nocera, Irene, Carlotta Bocci, Carlo Cantile, Moroni, Rebecca   +15 more
core   +1 more source

Congenital Skin Sloughing in the Setting of Hydrops Fetalis Secondary to Congenital Diffuse Lymphangiectasia Mimicking Epidermolysis Bullosa

Pediatric Dermatology, EarlyView.
ABSTRACT We present a case where the combination of severe hydrops fetalis, lymphangiectasia, and skin desquamation created a clinical picture that masqueraded as epidermolysis bullosa (EB). A neonate presented at birth with severe hydrops fetalis and extensive skin sloughing.
Sophia Rafferty, Kate L. Wilson, Jennifer B. Mancuso, Nicole Larsen, Grace A. Osborne, Jacqueline Meadow   +5 more
wiley   +1 more source

Fetal Parvowirus B19 infection with hydrops fetalis, a case report [PDF]

, 1970
Parvovirus B 19 (B19V) infection during pregnancy is a cause of nonimmune hydrops. We report a case of hydrops fetalis with severe fetal anemia in the course of B19V infection in the third trimester of pregnancy.
Grabarczyk, Piotr, Celewicz, Zbigniew, Grzymała-Figura, Anna, Engel, Karina, Węgrzynowski, Jan, Brojer, Ewa   +5 more
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