Top Abstract Purchase Related
Home
>
Node
>
Subnode

Dapsone-induced methemoglobinemia and hemolysis in the presence of familial hemoglobinopathy Hasharon and familial methemoglobin reductase deficiency

Ganer, A.; Knobel, B.; Fryd, C.H.; Rachmilewitz, E.A.

Israel Journal of Medical Sciences 17(8): 703-704

1981

ISSN/ISBN: 0021-2180
PMID: 6765904
Document Number: 180747
Methemoglobinemia and hemolysis are well-known side effects after using high doses of dapsone (4,4'-diaminodiphenylsulfone). Their occurrence after low doses of the drug, and subsequent investigation, revealed the presence of hemoglobin Hasharon, and low content of NADH-dependent methemoglobin reductase in five members of an East European ashkenazic Jewish family.

Document emailed within 1 workday
Secure & encrypted payments

Jabłońska-Skwiecińska, E.; Holtorp-Tyszkiewiczowa, J.; Staniszewska, K. 1984: Generalized deficiency of the NADH-methemoglobin reductase in congenital methemoglobinemia with neurological symptoms Biomedica Biochimica Acta 43(6): S98-100
Jabłońska-Skwiecińska, E.; Wierzbicka, M.; Kubicka, K. 1989: Cyanosis in children caused by inherited methemoglobinemia due to deficiency of NADH-dependent methemoglobin reductase in erythrocytes Pediatria Polska 64(1): 53-59
Kurz, R.; Hohenwallner, W. 1970: Familial glutathione reductase deficiency and disorder of glutathione synthesis in the erythrocyte Helvetica Paediatrica Acta 25(5): 542-552
Kaplan, J.C.; Junien, C.; Leroux, A.; Bamberger, J.; Bakouri, S.; Boué, J.; Boué, A. 1981: Prenatal diagnosis of generalized cytochrome b5 reductase deficiency (congenital methemoglobinemia with mental retardation, type II) Annales de Medecine Interne 132(2): 93-96
Li, N.; Boulay, M. 2010: Individual, familial and extra-familial factors associated with premarital sex among Bangladeshi male adolescents Sexual Health 7(4): 471-477
Krapivner, S.R.; Malyshev, P.P.; Rozhkova, T.A.; Potaraus, A.B.; Kukharchuk, V.V.; Bochkov, V.N. 2000: Application of DNA analysis for differential diagnosis of familial hypercholesterolemia and familial defect of apolipoprotein b-100 Terapevticheskii Arkhiv 72(4): 9-12
Akulenko, L.V.; Nikogosian, S.O.; Zhordaniia, K.I.; Kozachenko, V.P. 1991: Clinical course of the disease in familial and non-familial forms of serous cystadenocarcinoma of the ovary Akusherstvo i Ginekologiia 9: 58-60
Glueck, C.J.; Gartside, P.; Fallat, R.W.; Sielski, J.; Steiner, P.M. 1976: Longevity syndromes: familial hypobeta and familial hyperalpha lipoproteinemia Journal of Laboratory and Clinical Medicine 88(6): 941-957
Remacha, A.F.; del Río, E.; Baiget, M. 1998: Atypical familial microcytosis: a familial and genetic study Medicina Clinica 110(5): 183-185
Nell, P.A.; Ammann, A.J.; Hong, R.; Stiehm, E.R. 1972: Familial selective IgA deficiency Pediatrics 49(1): 71-79
Herranz Fernández, J.L.; Moreno Belzue, C.; Arce García, J.L.; Arteaga Manjón-Cabeza, R. 1992: Congenital familial hemiparesis and familial porencephaly Anales Espanoles de Pediatria 37(5): 431-433
Vicente, V.; Alberca, I.; Castro, M.; Goyenechea, A.; López Borrasca, A. 1987: Familial thrombosis caused by protein S deficiency Medicina Clinica 88(11): 459-462
Watel, A.; Goudemand, J.; Zandecki, M.; Laisne, C.; Bertrand, M.E.; Cosson, A. 1978: Familial antithrombin IIi deficiency and thromboembolic disease Lille Medical: Journal de la Faculte de Medecine et de Pharmacie de l'Universite de Lille 23(8): 555-560
Ploier, R.; Tappeiner, G.; Spaeth, P.; Emhofer, J. 1993: Familial lupus erythematosus with partial C4 deficiency Wiener Klinische Wochenschrift 105(11): 323-326
Rubinowitz, M.J.; Ford, C. 1977: Familial antithrombin IIi deficiency. An important clinical entity Rocky Mountain Medical Journal 74(5): 246-249
Voigtländer, V.; Bahmer, F.; Hauptmann, G. 1984: Familial discoid lupus erythematosus associated with heterozygous C4 deficiency Acta Dermato-Venereologica 64(6): 552-554
Miller, E.E.; Bowerman, D.L. 1976: Glomerulitis and factor vii deficiency in Familial Mediterranean fever Rocky Mountain Medical Journal 73(1): 25-30
Prusek, W.; Kotschy, M.; Podwysocka-Harasimowicz, M. 1979: Familial hemorrhagic diathesis caused by factor X deficiency Polski Tygodnik Lekarski 34(43): 1669-1670
Chaudhry, T.Anjum.; Adil, A.; Kazmi, F.; Ahmad, K. 2012: Familial presence of early onset Fuchs' corneal endothelial dystrophy, a report of two rare cases Jpma. Journal of the Pakistan Medical Association 62(7): 728-730
Arranz Peña, M.L.; Alonso de la Peña, M.C. 1985: Hyperlipoproteinemia type I. Study of a familial deficiency of lipoprotein-lipase Revista Clinica Espanola 176(2): 98-100