Zachmann M, Fuchs E, Prader A
Department of Paediatrics, University of Zurich, Kinderspital, Switzerland.
Eur J Pediatr. 1992 Mar;151(3):167-9. doi: 10.1007/BF01954375.
In an earlier report, we found that X-linked congenital adrenal hypoplasia may be associated with gonadotrophin deficiency. This combination has since been confirmed by many others. At the last examination, our patients were 22.4, 19.9 and 17.5 years old. They were doing well on replacement therapy with hydrocortisone, fluorohydrocortisone, and long-acting testosterone, but in all of them, a progressive hearing loss had appeared, starting at high frequencies at about 14 years of age. The loss progressed with age to lower frequencies, and the oldest patient had some remaining hearing capacity at 125-500 Hz only with a perceptive hearing loss of -95 dB at frequencies above 500 Hz. It is concluded that patients with this syndrome should be examined for hearing loss. X-linked adrenal hypoplasia may also be associated with glycerol kinase deficiency and myopathy. A molecular XP-deletion has suggested a locus for hypogonadotrophic hypogonadism distal to the glycerol kinase and adrenal hypoplasia loci. The observations in our patients suggest that the locus for at least this type of X-linked deafness may be in the same area.
在一份较早的报告中,我们发现X连锁先天性肾上腺发育不全可能与促性腺激素缺乏有关。此后,许多其他人也证实了这种联合情况。上次检查时,我们的患者年龄分别为22.4岁、19.9岁和17.5岁。他们在接受氢化可的松、氟氢可的松和长效睾酮替代治疗后情况良好,但他们所有人都出现了渐进性听力损失,大约在14岁时从高频开始。这种听力损失随着年龄增长扩展到低频,最年长的患者仅在125 - 500赫兹仍有一些听力,在500赫兹以上频率的感音神经性听力损失为 - 95分贝。得出的结论是,患有这种综合征的患者应接受听力损失检查。X连锁肾上腺发育不全也可能与甘油激酶缺乏和肌病有关。一种分子XP缺失提示了一个位于甘油激酶和肾上腺发育不全基因座远端的低促性腺激素性性腺功能减退基因座。我们患者的观察结果表明,至少这种类型的X连锁耳聋基因座可能在同一区域。