Kamoun P, Fensom A H, Shin Y S, Bakker E, Colombo J P, Munnich A, Bird S, Canini S, Huijmans J G, Chadefaux-Vekemans B
Laboratory of Biochemistry, URA CNRS 1335, Hôpital Necker-Enfants Malades, Paris, France.
Am J Med Genet. 1995 Jan 16;55(2):247-50. doi: 10.1002/ajmg.1320550220.
A European survey of prenatal diagnosis cases involving urea cycle diseases was performed. Citrullinemia was the most frequently investigated disease (108 cases). Other diseases are, in order of frequency, argininosuccinic aciduria (75 cases), ornithine transcarbamylase defect (52 cases), carbamoylphosphate synthetase defect (8 cases), triple H (3 cases), and arginase deficiency (1 case). Only one disease (ornithine transcarbamylase defect) is presently diagnosed using molecular biology methods.
开展了一项针对涉及尿素循环疾病的产前诊断病例的欧洲调查。瓜氨酸血症是调查最为频繁的疾病(108例)。其他疾病按出现频率依次为精氨琥珀酸尿症(75例)、鸟氨酸转氨甲酰酶缺陷(52例)、氨甲酰磷酸合成酶缺陷(8例)、三联征H(3例)和精氨酸酶缺乏症(1例)。目前仅有一种疾病(鸟氨酸转氨甲酰酶缺陷)采用分子生物学方法进行诊断。