Results 81 to 90 of about 26,761 (285)
A Preterm Infant with Gene Mutation Presenting with Cardiac Tamponade and Hydrops Fetalis: A Case Report [PDF]
Neonatal MedicineHydrops fetalis is a condition characterized by excessive fluid accumulation in the fetus, and is classified into immune and non-immune types depending on the underlying disease. Among cases of non-immune hydrops fetalis (NIHF), 15% to 20% are of cardiac
Jae Hun Jeong +2 more
doaj +1 more source
Hematological Indices of Parents in Non-Immune Hydrops Fetalis Pregnancie
Journal of Family and Reproductive Health, 2008 Objective:To investigate the hematologic indices of mothers in non-immune hydrops fetalis pregnancies and identify the possible causative role of Alpha-Thalassemia among them.
Saeed Reza Ghaffari +7 more
doaj
Hematology. American Society of Hematology. Education Program, 2018 The α-thalassemia trait, associated with deletions removing both α-globin genes from 1 chromosome (genotype ζ αα/ζ--), is common throughout Southeast Asia.
Andrew King, D. Higgs
semanticscholar +1 more source
Recém-nascido com hidrópsia fetal não imune - experiência de um centro de referência.
Acta Médica Portuguesa, 2008 Nonimmune hydrops fetalis is a rare affection that can result from several disorders. Notwithstanding with the advances in the diagnosis and treatment, its morbidity and mortality are still very high.
Ana Teixeira +3 more
doaj +1 more source
Haematologica, 2018 Diamond-Blackfan anemia (DBA) is a rare inherited bone marrow failure disorder linked predominantly to ribosomal protein gene mutations. Here the European DBA consortium reports novel mutations identified in the RPL15 gene in 6 unrelated individuals ...
M. Wlodarski +19 more
semanticscholar +1 more source
Homozygosity for the Mediterranean a-thalassemic deletion (hemoglobin Barts hydrops fetalis)
Annals of Saudi Medicine, 2010 Hemoglobin Barts hydrops fetalis syndrome is the most severe and generally fatal clinical phenotype of α-thalassemia. We diagnosed a fetus at 23-weeks gestation with having hydrops fetalis, by ultrasound. At 32 weeks, intrauterine death was detected.
Al-Allawi Nasir +2 more
doaj
Newborn and Infant Nursing Reviews, 2006 Newborn and Infant Nursing Reviews 6 (2006) e1-e8. doi:10.1053/j.nainr.2006.05.006 ; Received by publisher: 0000-01-01 ; Harvest Date: 2016-01-04 12:23:39 ; DOI:10.1053/j.nainr.2006.05.006 ; Page Range: e1 ...
College of Nursing, University of Florida, Gainesville, FL ( host institution ) +1 more
openaire +2 more sources
An approach to familial lymphoedema. [PDF]
, 2017 Lymphoedema is the build-up of lymphatic fluid leading to swelling in the tissues. Most commonly it affects the peripheries. Diagnosis is based on clinical assessment and imaging with lymphoscintigraphy. Treatment is supportive with compression garments,
Atton +4 more
core +1 more source
Non-progressive Non-immune Hydrops Fetalis Caused by a Novel Mutation in GUSB Gene [PDF]
, 2020 Mucopolysaccharidosis type VII or Sly syndrome is a rare autosomal recessive disorder caused by deficiency of β Glucuronidase enzyme, which is involved in degradation of glycosaminoglycans.
Alaei, Mohammadreza +4 more
core +2 more sources
Case report: Giant congenital pulmonary airway malformation initially managed and resected on ECMO
Journal of Pediatric Surgery Case Reports, 2016 Congenital pulmonary airway malformations (CPAM) are a common congenital anomaly, occurring as a result of aberrant formation of pulmonary lobes or segments. Many patients with CPAM are treated with postnatal surgical excision within 1-year of age.
Richard Yeker +3 more
doaj +1 more source