Comparison of quantitative and qualitative tests for glucose-6-phosphate dehydrogenase deficiency in the neonatal period

2017 ◽  
Vol 39 (3) ◽  
pp. 251-260 ◽  
Author(s):  
F. Keihanian ◽  
S. Basirjafari ◽  
B. Darbandi ◽  
A. Saeidinia ◽  
M. Jafroodi ◽  
...  
Keyword(s):  
Dehydrogenase Deficiency ◽  
Neonatal Period ◽  
Glucose 6 Phosphate Dehydrogenase

scholarly journals Comparison of Commercial Screening Tests for Glucose-6-Phosphate Dehydrogenase Deficiency in the Neonatal Period

1997 ◽  
Vol 43 (7) ◽  
pp. 1236-1237 ◽  
Author(s):  
Michael Kaplan ◽  
Chava Leiter ◽  
Cathy Hammerman ◽  
Bernard Rudensky
Keyword(s):  
Dehydrogenase Deficiency ◽  
Neonatal Period ◽  
Screening Tests ◽  
Glucose 6 Phosphate Dehydrogenase

scholarly journals Severe Presentation of Congenital Hemolytic Anemias in the Neonatal Age: Diagnostic and Therapeutic Issues

Diagnostics ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 1549 ◽  
Author(s):  
Valeria Cortesi ◽  
Francesca Manzoni ◽  
Genny Raffaeli ◽  
Giacomo Cavallaro ◽  
Bruno Fattizzo ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Dehydrogenase Deficiency ◽  
Hereditary Spherocytosis ◽  
Neonatal Period ◽  
Reticulocyte Count ◽  
Fetal Hemoglobin ◽  
Peripheral Blood Smear ◽  
Unconjugated Hyperbilirubinemia ◽  
High Index Of Suspicion ◽  
Glucose 6 Phosphate Dehydrogenase

Congenital hemolytic anemias (CHAs) are a group of diseases characterized by premature destruction of erythrocytes as a consequence of intrinsic red blood cells abnormalities. Suggestive features of CHAs are anemia and hemolysis, with high reticulocyte count, unconjugated hyperbilirubinemia, increased lactate dehydrogenase (LDH), and reduced haptoglobin. The peripheral blood smear can help the differential diagnosis. In this review, we discuss the clinical management of severe CHAs presenting early on in the neonatal period. Appropriate knowledge and a high index of suspicion are crucial for a timely differential diagnosis and management. Here, we provide an overview of the most common conditions, such as glucose-6-phosphate dehydrogenase deficiency, pyruvate kinase deficiency, and hereditary spherocytosis. Although rare, congenital dyserythropoietic anemias are included as they may be suspected in early life, while hemoglobinopathies will not be discussed, as they usually manifest at a later age, when fetal hemoglobin (HbF) is replaced by the adult form (HbA).

Glucose-6-Phosphate Dehydrogenase Deficiency in an Old Woman

2020 ◽  
Vol 6 (3) ◽  
Author(s):  
Briantais Antoine ◽  
Froidefond Margaux ◽  
Seguier Julie ◽  
Swiader Laure ◽  
Durand Jean Marc
Keyword(s):  
Dehydrogenase Deficiency ◽  
Glucose 6 Phosphate Dehydrogenase

Diversity in expression of glucose-6-phosphate dehydrogenase deficiency in females

1999 ◽  
Vol 55 (1) ◽  
pp. 13-19 ◽  
Author(s):  
Yousef M Abdulrazzaq ◽  
Rosette Micallef ◽  
M Mansoor Qureshi ◽  
Adekunle Dawodu ◽  
Ibrahim Ahmed ◽  
...  
Keyword(s):  
Dehydrogenase Deficiency ◽  
Glucose 6 Phosphate Dehydrogenase

Three mutations analysis of glucose-6-phosphate dehydrogenase deficiency in neonates in South-west China

2007 ◽  
Vol 49 (4) ◽  
pp. 463-467
Author(s):  
CHUN DENG ◽  
CHUN-BAO GUO ◽  
YOU-HUA XU ◽  
BING DENG ◽  
JIA-LIN YU
Keyword(s):  
Dehydrogenase Deficiency ◽  
West China ◽  
South West ◽  
Glucose 6 Phosphate Dehydrogenase
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