Results 211 to 220 of about 26,761 (285)
Immunologic and nonimmunologic hydrops fetalis
M Tuncer, G Erdem, O Oran
doaj
Lysosomal storage disorders as an etiology of nonimmune hydrops fetalis: A systematic review [PDF]
We performed a systematic review of the literature to evaluate the incidence and types of lysosomal storage disorders (LSD) in case series of nonimmune hydrops fetalis (NIHF).
N. Iyer+4 more
semanticscholar +2 more sources
Nonimmune hydrops fetalis (NIHF) poses a significant challenge in perinatal care due to its high mortality rates and diverse etiologies. This comprehensive review examines the pathophysiology, etiology, antenatal diagnosis and management, postnatal care, and outcomes of NIHF. NIHF arises from numerous underlying pathologies, including genetic disorders,
Shannon B, Dunn, Julie R, Whittington
openaire +3 more sources
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The many etiologies of nonimmune hydrops fetalis diagnosed by exome sequencing
Prenatal Diagnosis, 2021To explain the importance of identifying an etiology for the pathological finding of nonimmune hydrops fetalis (NIHF) and to explore the impact of exome sequencing in recurrent NIHF.
T. Wagner+9 more
semanticscholar +1 more source
Prenatal Diagnosis, 2021
Nonimmune hydrops fetalis (NIHF) has varied etiology. We assessed the etiological spectrum and evaluated the utility of fetal whole exome sequencing (fWES) for the diagnosis of NIHF.
Alec Reginald Errol Correa+7 more
semanticscholar +1 more source
Nonimmune hydrops fetalis (NIHF) has varied etiology. We assessed the etiological spectrum and evaluated the utility of fetal whole exome sequencing (fWES) for the diagnosis of NIHF.
Alec Reginald Errol Correa+7 more
semanticscholar +1 more source
Outcomes of allogeneic transplantation for hemoglobin Bart’s hydrops fetalis syndrome in Hong Kong
Pediatric Transplantation, 2021Hemoglobin Bart's hydrops fetalis syndrome (BHFS) was once considered a fatal condition universally. Medical advances over the past three decades have resulted in increasing numbers of BHFS survivors.
W. Y. Chan+6 more
semanticscholar +1 more source
Hemoglobin, 2021
α0-Thalassemia (α0-thal) Chiang Rai (– –CR; NC_000016.10: g.144215_188843del) was identified as a novel 44.6 kb deletional type of α-thalassemia (α-thal), removing all α-like globin genes.
C. Ruengdit+3 more
semanticscholar +1 more source
α0-Thalassemia (α0-thal) Chiang Rai (– –CR; NC_000016.10: g.144215_188843del) was identified as a novel 44.6 kb deletional type of α-thalassemia (α-thal), removing all α-like globin genes.
C. Ruengdit+3 more
semanticscholar +1 more source
Clinics in Perinatology, 2000
Although most NIH fetuses have poor prognosis, it is imperative to attempt to identify the underlying cause to present parents with the best estimate for prognosis and future outcomes. Identification of a disorder with a good prognosis may prevent unnecessary termination of pregnancy and give a chance for therapy. Identification of a disorder with poor
R, Bukowski, G R, Saade
openaire +2 more sources
Although most NIH fetuses have poor prognosis, it is imperative to attempt to identify the underlying cause to present parents with the best estimate for prognosis and future outcomes. Identification of a disorder with a good prognosis may prevent unnecessary termination of pregnancy and give a chance for therapy. Identification of a disorder with poor
R, Bukowski, G R, Saade
openaire +2 more sources
Nonimmunologic hydrops fetalis
American Journal of Obstetrics and Gynecology, 1984Twenty cases of nonimmunologic hydrops fetalis were reviewed. The incidence of nonimmunologic hydrops fetalis was 1/2,029 (20 cases in 40,588 deliveries). The diverse etiologies of nonimmunologic hydrops fetalis are demonstrated. The incidence of erythroblastosis fetalis caused by Rh isoimmunization declined markedly.
Seung Soon Im+4 more
openaire +3 more sources
Nonimmune hydrops fetalis and congenital disorders of glycosylation: A systematic literature review
Journal of Inherited Metabolic Disease, 2020Numerous etiologies may lead to nonimmune hydrops fetalis (NIHF) including congenital disorders of glycosylation (CDG). Recognition of CDG in NIHF is challenging. This study reviews prenatal and neonatal characteristics of CDG presenting with NIHF.
Mona M Makhamreh+4 more
semanticscholar +1 more source