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Kallmann氏综合征于1944年被正式命名,国内所见病例不多。近几年来,孟荟、李永梅等已先后作过报道,均以继发性睾丸机能低下、嗅觉障碍、其他先天畸形等综合症群为主要组合形式。现将本组四例Kallmann氏综合征报告如下: 病例1 男性,23岁。因阴茎、睾丸发育不良于1990年9月5日入院。患者自诉偶有性欲要求,夜间阴茎可勃起,无梦遗,手淫不排精。同胞兄弟身材高于患者本人约10cm,其父嗅觉不灵敏;有一外甥的阴茎、睾丸比同龄人细小。查:智力正常,身高160cm,指距168cm,体重46kg。视力及色觉正常,无周边视野缺损。不能辨别碘酒、食醋的气味,对二甲苯的气味反应迟钝。皮肤及粘膜无色素沉着,无喉结,无胡须,腋毛及阴毛稀少。阴
Kallmann’s syndrome was officially named in 1944, few cases of domestic see. In recent years, Meng Hui, Li Yongmei, etc. have been reported, are secondary to testicular dysfunction, olfactory dysfunction, other congenital malformations and other syndromes as the main combination. Now this group of four cases of Kallmann’s syndrome report as follows: Case 1 male, 23 years old. Due to the penis, testicular dysplasia in September 5, 1990 admission. Patient self-prosecution occasional sexual desire, night penile erection, no dreams, masturbation is not exclusive. Sister brother is taller than the patient himself about 10cm, his father smell insensitive; there is a nephew of the penis, testes smaller than their peers. Check: mental normal, height 160cm, finger distance 168cm, weight 46kg. Normal vision and color vision, no peripheral visual field defects. Can not distinguish between iodine, vinegar odor, paraxylylene odor unresponsive. No skin pigmentation and mucosa, no Adam’s apple, no beard, armpit hair and pubic hair scarce. yin