Echenne B, Ferran J L
Pediatrie. 1985 Jun;40(4):313-7.
The diagnosis of Weaver-Smith syndrome has been carried out on two patients with facial dysmorphic features, excessive growth and accelerated bone maturation. A marked spasticity of the lower limbs with joint contractures in one patient, a spastic quadriplegia with delayed milestones in the second patient were the most prominent clinical features. In both cases a spontaneous improvement of muscle tone with complete recovery was observed at the end of the first year of life.
对两名有面部畸形特征、生长过度和骨骼成熟加速的患者进行了韦弗-史密斯综合征的诊断。一名患者下肢明显痉挛并伴有关节挛缩，另一名患者为痉挛性四肢瘫痪且发育里程碑延迟，这些是最突出的临床特征。在这两个病例中，在出生后第一年年底均观察到肌张力自发改善并完全恢复。
