scholarly journals Diabetic ketoacidosis does not precipitate haemolysis in patients with the Mediterranean variant of glucose-6-phosphate dehydrogenase deficiency.

BMJ ◽  
1984 ◽  
Vol 288 (6412) ◽  
pp. 179-180 ◽  
Author(s):  
O Shalev ◽  
A Wollner ◽  
J Menczel
Keyword(s):  
Diabetic Ketoacidosis ◽  
Dehydrogenase Deficiency ◽  
The Mediterranean ◽  
Glucose 6 Phosphate Dehydrogenase

scholarly journals Genetic diversity of the “Mediterranean” glucose-6-phosphate dehydrogenase deficiency phenotype

1971 ◽  
Vol 50 (6) ◽  
pp. 1253-1261 ◽  
Author(s):  
George Stamatoyannopoulos ◽  
Volker Voigtlander ◽  
Panayotis Kotsakis ◽  
Angelos Akrivakis
Keyword(s):  
Genetic Diversity ◽  
Dehydrogenase Deficiency ◽  
The Mediterranean ◽  
Glucose 6 Phosphate Dehydrogenase

scholarly journals Primary thrombocythemia: clonal origin of platelets, erythrocytes, and granulocytes in a GdB/GdMediterranean subject

Blood ◽  
1982 ◽  
Vol 59 (1) ◽  
pp. 76-79 ◽  
Author(s):  
GF Gaetani ◽  
AM Ferraris ◽  
S Galiano ◽  
P Giuntini ◽  
L Canepa ◽  
...  
Keyword(s):  
T Lymphocytes ◽  
Somatic Cell ◽  
Essential Thrombocythemia ◽  
Dehydrogenase Deficiency ◽  
Myeloproliferative Disorder ◽  
Primary Thrombocythemia ◽  
Normal Glucose ◽  
Clonal Origin ◽  
The Mediterranean ◽  
Glucose 6 Phosphate Dehydrogenase

A patient with primary thrombocythemia, who was heterozygous for glucose-6-phosphate dehydrogenase deficiency (GdB/GdMed), was investigated to test for the clonal origin of this myeloproliferative disorder. In order to assess somatic cell mosaicism in various tissues, we have made use of the different rate of utilization of 2-deoxyglucose- 6-phosphate, an analog of glucose-6-phosphate, by normal glucose-6- phosphate dehydrogenase and by the Mediterranean variant: the results demonstrate that essential thrombocythemia is a clonal disease involving the erythrocytic, granulocytic, and megakaryocytic series, without affecting monocytes, T lymphocytes, and non-T lymphocytes.

scholarly journals Primary thrombocythemia: clonal origin of platelets, erythrocytes, and granulocytes in a GdB/GdMediterranean subject

Blood ◽  
1982 ◽  
Vol 59 (1) ◽  
pp. 76-79 ◽  
Author(s):  
GF Gaetani ◽  
AM Ferraris ◽  
S Galiano ◽  
P Giuntini ◽  
L Canepa ◽  
...  
Keyword(s):  
T Lymphocytes ◽  
Somatic Cell ◽  
Essential Thrombocythemia ◽  
Dehydrogenase Deficiency ◽  
Myeloproliferative Disorder ◽  
Primary Thrombocythemia ◽  
Normal Glucose ◽  
Clonal Origin ◽  
The Mediterranean ◽  
Glucose 6 Phosphate Dehydrogenase

Abstract A patient with primary thrombocythemia, who was heterozygous for glucose-6-phosphate dehydrogenase deficiency (GdB/GdMed), was investigated to test for the clonal origin of this myeloproliferative disorder. In order to assess somatic cell mosaicism in various tissues, we have made use of the different rate of utilization of 2-deoxyglucose- 6-phosphate, an analog of glucose-6-phosphate, by normal glucose-6- phosphate dehydrogenase and by the Mediterranean variant: the results demonstrate that essential thrombocythemia is a clonal disease involving the erythrocytic, granulocytic, and megakaryocytic series, without affecting monocytes, T lymphocytes, and non-T lymphocytes.

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
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