de Verneuil H, Aitken G, Nordmann Y
Hum Genet. 1978 Oct 31;44(2):145-51. doi: 10.1007/BF00295407.
Uroporphyrinogen (URO) decarboxylase was measured in hemoglobin-free erythrocytes from subjects with familial porphyria cutanea: the mean activity was about 50% of that found in erythrocytes from normal subjects. Asymptomatic carriers were always found in the family. No enzyme deficiency was found in erythrocytes from subjects with sporadic porphyria cutanea. The measurement of URO decarboxylase in erythrocytes seems to allow an easy distinction between these two groups of porphyria cutanea.
对患有家族性迟发性皮肤卟啉症患者的无血红蛋白红细胞中的尿卟啉原(URO)脱羧酶进行了测定:平均活性约为正常受试者红细胞中该酶活性的50%。该家族中总是能发现无症状携带者。散发性迟发性皮肤卟啉症患者的红细胞中未发现酶缺乏。红细胞中URO脱羧酶的测定似乎有助于轻松区分这两组迟发性皮肤卟啉症。