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西班牙伴有红细胞嘧啶5'-核苷酸酶缺乏的遗传性溶血性贫血。临床、生物学及家族研究

Hereditary hemolytic anemia with erythrocyte pyrimidine 5'-nucleotidase deficiency in Spain. Clinical, biological and familial studies.

作者信息

Vives-Corrons J L, Montserrat-Costa E, Rozman C

出版信息

Hum Genet. 1976 Dec 15;34(3):285-92. doi: 10.1007/BF00295292.

Abstract

We report a hereditary hemolytic anemia associated with a severe erythrocyte pyrimidine 5'-nucleotidase deficiency in a Spanish family of five members in which the parents are first cousins. Both parents exhibited decreased nucleotidase activity without clinical or hematologic abnormalities. Two children (a male and a female) showed severe pyrimidine 5'-nucleotidase deficiency with hemolytic anemia. The remaining child (a male) showed no signs of the disease. The findings strongly suggest an autosomal recessive mode of inheritance in this enzymopathy. This seems to be the first report of pyrimidine 5'-nucleotidase deficiency in Spain.

摘要

我们报告了一个西班牙五口之家的遗传性溶血性贫血病例,该病例与严重的红细胞嘧啶5'-核苷酸酶缺乏症相关,其父母为近亲。父母双方的核苷酸酶活性均降低,但无临床或血液学异常。两个孩子(一男一女)表现出严重的嘧啶5'-核苷酸酶缺乏症并伴有溶血性贫血。另一个孩子(男性)未表现出该病症状。这些发现强烈提示这种酶病为常染色体隐性遗传模式。这似乎是西班牙关于嘧啶5'-核苷酸酶缺乏症的首例报告。

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