Wilson J D, Griffin J E, Russell D W
Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas 75235.
Endocr Rev. 1993 Oct;14(5):577-93. doi: 10.1210/edrv-14-5-577.
In the 20 yr since it was established that impairment of dihydrotestosterone formation is the cause of a rare form of human intersex, a wealth of information has accumulated about the genetics, endocrinology, and variable phenotypic manifestations, culminating in the cloning of cDNAs encoding two 5 alpha-reductase genes and documentation that mutations in the steroid 5 alpha-reductase 2 gene are the cause of 5 alpha-reductase deficiency. Perplexing and difficult problems remain unresolved, e.g. whether the variability in manifestations is due to variable expressions of steroid 5 alpha-reductase 1 or to effects of testosterone itself. It is also imperative to establish whether defects in steroid 5 alpha-reductase 2, perhaps in the heterozygous state, are responsible for a portion of cases of sporadic hypospadias, to determine whether 5 alpha-reductase plays a role in progesterone action in women, and to elucidate the relation between androgen action and gender role behavior.
自从确定二氢睾酮生成受损是人类一种罕见的两性畸形形式的病因以来的20年里,已经积累了大量关于遗传学、内分泌学以及可变表型表现的信息,最终克隆出了编码两种5α-还原酶基因的cDNA,并证明类固醇5α-还原酶2基因的突变是5α-还原酶缺乏症的病因。令人困惑和棘手的问题仍然没有得到解决,例如,表现的变异性是由于类固醇5α-还原酶1的可变表达还是由于睾酮本身的作用。确定类固醇5α-还原酶2的缺陷(可能处于杂合状态)是否导致一部分散发性尿道下裂病例,确定5α-还原酶在女性孕酮作用中是否起作用,以及阐明雄激素作用与性别角色行为之间的关系也势在必行。