Doman A N, Maroteaux P, Lyne E D
Hôpital des Enfants Malades, Paris, France.
J Bone Joint Surg Am. 1990 Oct;72(9):1364-9.
The cases of four patients who had an unusual clinical entity of disproportionately short stature, referred to as spondyloepiphyseal dysplasia of Maroteaux, are described. In patients who have this syndrome, the abnormalities are confined to the musculoskeletal system. The patients do not have corneal opacities or increased excretion of keratosulphate. The mode of transmission appears to be autosomal dominant. Platyspondylysis is present but there are no anterior tongue-like deformities of the vertebral bodies. Because of the presence of spondyloepiphyseal dysplasia and normal intelligence, and the lack of abnormalities at birth, this entity seems to mimic Morquio syndrome. However, unlike Morquio syndrome, the disorder involves no biochemical abnormalities. Thus, the entity may be classified as new.
本文描述了四名患有一种不寻常临床病症(称为马罗托克斯脊椎骨骺发育不良)的患者病例,该病症患者身材极短。患有此综合征的患者,异常情况局限于肌肉骨骼系统。患者没有角膜混浊或硫酸角质素排泄增加的情况。遗传方式似乎为常染色体显性遗传。存在扁平椎体溶解,但椎体没有前舌状畸形。由于存在脊椎骨骺发育不良且智力正常,且出生时无异常,此病症似乎类似黏多糖贮积症IV型。然而,与黏多糖贮积症IV型不同,该病症不涉及生化异常。因此,此病症可归类为一种新病症。