Meinecke P, Schaefer E, Engelbrecht R
Eur J Pediatr. 1983 Oct;141(1):58-9. doi: 10.1007/BF00445673.
This paper reports the first female case of the Weaver syndrome. The prominent clinical features are gigantism, macrocephaly, and the characteristic facial dysmorphism. Hypertonia and bone maturation acceleration are somewhat less pronounced than in the formerly published cases of male patients. The etiology of the syndrome remains unclear, but if genetic, X-linked recessive inheritance can be excluded.
本文报道了第一例女性韦弗综合征病例。其突出的临床特征为巨人症、巨头畸形以及特征性面部畸形。与之前报道的男性患者病例相比,肌张力亢进和骨骼成熟加速的表现略显不那么明显。该综合征的病因尚不清楚,但如果是遗传性的,可以排除X连锁隐性遗传。