Results 81 to 90 of about 21,398 (250)
Alpha-thalassaemic hydrops fetalis. [PDF]
Archives 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
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
JIMD Reports, 2019 Multiple sulfatase deficiency (MSD) is an ultra‐rare lysosomal storage disorder (LSD). Mutations in the SUMF1 gene encoding the formylglycine generating enzyme (FGE) result in an unstable FGE protein with reduced enzymatic activity, thereby affecting the
Lars Schlotawa +6 more
semanticscholar +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
Mirror Syndrome Leading to Eclampsia in a Pregnant Woman: a case report [PDF]
Majallah-i Zanān, Māmā̓ī va Nāzā̓ī-i Īrān, 2018 Introduction: Mirror syndrome is described as mother's generalized edema accompanied with hydrops fetalis, which sometimes leads to preeclampsia. Mirror syndrome is uncommon and its accompaniment with eclampsia is very rare.
Nayereh Ghomian +2 more
doaj +1 more source
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
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
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
, 2010 Alpha-thalassaemia is inherited as an autosomal recessive disorder characterised by a microcytic hypochromic anaemia, and a clinical phenotype varying from almost asymptomatic to a lethal haemolytic ...
A Cao +141 more
core +3 more sources
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