Al Herbish A S, Al Jurayyan N A, Abo Bakr A M, Abdullah M A, Al Husain M, Al Rabeah A A, Patel P J, Jawad A, Al Samarrai A I
Departments of Pediatrics, Surgery, and Radiology, King Khalid University Hospital, Department of Pediatrics, Security Forces Hospital, and Pediatric Surgery, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
Ann Saudi Med. 1996;16(1):12-5. doi: 10.5144/0256-4947.1996.12.
Sexual ambiguity is a complex and often confusing medical problem. In addition to the life-threatening adrenal crises which may accompany some forms, ambiguity of the genitalia may lead to incorrect sex assignment by parents and/or health personnel. Children who present to medical attention beyond the neonatal period constitute a challenging problem due to the grave consequences of this condition. Thirty cases in whom sex reassignment was indicated were seen at King Khalid University Hospital, Riyadh, over a 10-year period. Of these, 27 (90%) were genetic females (20 were 21- and seven were 11-hydroxylase deficient) and three (10%) were genetic males (two partial androgen insensitive and one 5alpha-reductase deficient). All genetic males who were incorrectly assigned as females accepted reassignment. But 9 out of 27 (33%) of the genetic females who were incorrectly assigned as males refused reassignment. Preference for male sex assignment, delayed diagnosis and sociocultural circumstances seem to be the contributing factors for refusal. A national consensus about this important issue strengthened by the existing religious recommendations in demanded.
性器官模糊是一个复杂且常常令人困惑的医学问题。除了某些类型可能伴随的危及生命的肾上腺危象外,生殖器模糊可能导致父母和/或医护人员对性别做出错误的认定。由于这种情况的严重后果,在新生儿期之后前来就医的儿童构成了一个具有挑战性的问题。在利雅得的哈立德国王大学医院,在10年期间共诊治了30例需要进行性别重新认定的病例。其中,27例(90%)为基因女性(20例为21-羟化酶缺乏,7例为11-羟化酶缺乏),3例(10%)为基因男性(2例为部分雄激素不敏感,1例为5α-还原酶缺乏)。所有被错误认定为女性的基因男性都接受了重新认定。但在27例被错误认定为男性的基因女性中,有9例(33%)拒绝重新认定。对男性性别认定的偏好、诊断延迟和社会文化环境似乎是拒绝的促成因素。需要通过现有的宗教建议加强对此重要问题的全国性共识。