. 2002; 17(1): 59-60 | |||
Hereditary MethemoglobinemiaTolga Yakar1, Nejat Altıntaş2, Atalay Surardamar1, Fatih Akdoğan1, Taha Tahir Bekçi11Haydarpasa Numune Hospital, Internal Medicine Clinic, Istanbul2SSK Sureyyapasa Hospital, Chest Diseases, Istanbul Hereditary methemoglobinemia is an autosomal dominant disorder which is due to either to the presence of one of the M hemoglobins or the deficiency of the enzyme cytochrome B5 reductase. Cytochromeb5 reductase reductase deficiency have lifelong cyanosis of variable degree, depending on the level of methemoglobin, but usually have no associated symptoms or other physical findings. Herediter MethemoglobinemiTolga Yakar1, Nejat Altıntaş2, Atalay Surardamar1, Fatih Akdoğan1, Taha Tahir Bekçi11Haydarpaşa Numune Hastanesi, İç Hastalıkları Kliniği, İstanbul2SSK Süreyyapaşa Hastanesi, Göğüs Hastalıkları Kliniği, İstanbul Anahtar Kelimeler: Herediter mnethemoglobinemi, sitokrom B5 reduktaz enzimi, hemoglobin M Tolga Yakar, Nejat Altıntaş, Atalay Surardamar, Fatih Akdoğan, Taha Tahir Bekçi. Hereditary Methemoglobinemia. . 2002; 17(1): 59-60 Corresponding Author: Nejat Altıntaş, Türkiye |
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