Malina L, Lim C K
Department of Dermatology, Faculty of Medical Hygiene, Charles University, Prague, Czechoslovakia.
Br J Dermatol. 1988 Feb;118(2):243-5. doi: 10.1111/j.1365-2133.1988.tb01781.x.
We report the case of a woman with hereditary porphyria cutanea tarda which manifested 3 weeks after she gave birth to her second child. The mother of the patient had also been diagnosed and treated for porphyria cutanea tarda. Reduced red cell uroporphyrinogen decarboxylase activity was found in the patient, the new-born child and the patient's mother. Normal enzyme activity was found in the patient's first child.
我们报告了一例迟发性皮肤卟啉病的女性病例，该病在她生下第二个孩子3周后出现。患者的母亲也曾被诊断为迟发性皮肤卟啉病并接受过治疗。在患者、新生儿和患者母亲中均发现红细胞尿卟啉原脱羧酶活性降低。在患者的第一个孩子中发现酶活性正常。
