Wraith J E, Danks D M, Rogers J G
Department of Genetics, Royal Children's Hospital, Parkville, VIC.
Med J Aust. 1987 Nov 2;147(9):450-1.
Sanfilippo syndrome (mucopolysaccharidosis type III) usually presents with severe behavioural disturbance and it has characteristic features. The patient's condition follows a neurodegenerative course; death generally occurs in the second decade. Five patients, from three families, who presented with a mild variety of the syndrome are reported here. Four of the five patients did not show the usual somatic features, and none showed regression. It is important that clinicians be aware of this mild variant so that appropriate tests can be undertaken in retarded children and adults.
桑菲利波综合征(黏多糖贮积症III型)通常表现为严重的行为障碍且具有特征性表现。患者病情呈神经退行性病程;通常在第二个十年期死亡。本文报告了来自三个家庭的五名患有该综合征轻度类型的患者。五名患者中有四名未表现出常见的躯体特征,且均未出现退化现象。临床医生了解这种轻度变异型很重要,以便能对智力发育迟缓的儿童和成人进行适当的检查。