Gaucher A, Netter P, Fuare G, Raffoux C, Chanson B, Baumgartner J, Psurel J, Streiff F
Rev Rhum Mal Osteoartic. 1977 Apr;44(4):273-7.
Study of urinary homogentisic acid and a determinantion of group HLA were carried out for 36 members of a family spread over three generations with three cases of ochronotic rheumatism in the second generation. Alkaptonuria was discovered in seven other subjects, six of them members of the third generation: urinary elimination was poor, less than 0.60 g/24 hours. There is a certain degree of consanguinity in the family studied here and these findings do not therefore rule out a recessive autosomal transmission of the alkaptonuria. They do however lead to the consideration that alkaptonuria may sometimes be found in heterozygotic subjects. A genetic relationship between HLA complex and alkaptonuria can only be claimed with difficulty from this familial study, but the high frequency of B 27 antigen (29 out of 36 members carring it) leaves room for the hypothesis that the B 27 gene, or more precisely a gene associated with the B 27 gene, plays a part in the development of ochronotic rheumatism.
对一个三代家族的36名成员进行了尿黑酸研究及HLA分型测定,该家族第二代有3例褐黄病性风湿。在其他7名受试者中发现了尿黑酸尿症,其中6名是第三代成员:尿排泄量低,低于0.60克/24小时。在此研究的家族中有一定程度的近亲结婚,因此这些发现不能排除尿黑酸尿症的常染色体隐性遗传。然而,这些发现确实促使人们考虑尿黑酸尿症有时可能在杂合子个体中出现。从这项家族研究中很难断言HLA复合体与尿黑酸尿症之间存在遗传关系,但B27抗原的高频率(36名成员中有29名携带)为以下假设留下了空间:B27基因,或者更确切地说,与B27基因相关的一个基因,在褐黄病性风湿的发展中起作用。