Kaiserman K B, Nakamoto J M, Geffner M E, McCabe E R
Department of Pediatrics, UCLA Children's Hospital 90095-1752, USA.
J Pediatr. 1998 Aug;133(2):300-2. doi: 10.1016/s0022-3476(98)70242-2.
An infant and his uncle, both with adrenal hypoplasia congenita, shared the same DAX1 mutation. The adolescent uncle had hypogonadotropic hypogonadism, but the infant had a normal minipuberty of infancy. These observations suggest differences in the physiologic mechanisms regulating the hypothalamic-pituitary-gonadal axis in infancy and adolescence.
一名婴儿及其叔叔均患有先天性肾上腺发育不全,且携带相同的DAX1基因突变。青少年叔叔患有促性腺激素缺乏性性腺功能减退,但婴儿在婴儿期有正常的小青春期。这些观察结果提示在婴儿期和青少年期调节下丘脑-垂体-性腺轴的生理机制存在差异。