Pennock C A, Gordon I R, Longdon K, Burman D
J Inherit Metab Dis. 1980;2(3):75-8. doi: 10.1007/BF01801723.
The clinical and radiological features of a patient with Kniest dysplasia, a form of metatropic dwarfism, are described. The patient excreted glycosaminoglycans (mucopolysaccharides) in normal amounts during infancy but subsequently showed abnormal keratan sulphate excretion. The significance of these findings and the possibility that Kniest dysplasia represent another mucopolysaccharidosis are discussed.
本文描述了一名患有Kniest发育不全(一种发育异常性侏儒症)患者的临床和放射学特征。该患者在婴儿期排泄的糖胺聚糖(粘多糖)量正常,但随后出现硫酸角质素排泄异常。文中讨论了这些发现的意义以及Kniest发育不全可能代表另一种粘多糖贮积症的可能性。