al-Attia H M, Bakir A M, Butt N J
Department of Internal Medicine, Mafraq Hospital, ABU Dhabi, U.A.E.
Acta Clin Belg. 1993;48(3):195-201. doi: 10.1080/17843286.1993.11718307.
Two forms of 5 alpha-reductase deficiency have been described and two genes have been cloned. In view of the psychoendocrinological complexity of the primary form, the early diagnosis preferably in infancy, is crucial. Rearing up those who are assigned as females to the male gender identity could minimize the risk of gender identity and role disorders when puberty is reached.
已经描述了两种形式的5α-还原酶缺乏症,并且克隆了两个基因。鉴于原发性形式的心理内分泌学复杂性,最好在婴儿期进行早期诊断至关重要。将那些被指定为女性的人培养成男性性别认同,可以在进入青春期时将性别认同和角色障碍的风险降至最低。