Young I D, Harper P S
Arch Dis Child. 1982 Nov;57(11):828-36. doi: 10.1136/adc.57.11.828.
The clinical features are described in 31 cases of the mild form of Hunter's syndrome (mucopolysaccharidosis II) ascertained in the British Isles. The mean age at onset was 4.3 years and at death was 21.7 years. Each patient had a large head and short stature. Umbilical and inguinal herniae were recorded in 95% and 61% of the cases. Evidence of cardiac disease was found in 91%; this was the most common cause of death. All of the patients suffered from frequent upper or lower respiratory tract infection. Middle airways obstruction proved to be a particular hazard. A high incidence of sensorineural deafness and unexplained papilloedema was noted. The importance of regular health care for these individuals is stressed.
本文描述了在不列颠群岛确诊的31例轻度亨特综合征(黏多糖贮积症II型)患者的临床特征。发病平均年龄为4.3岁,死亡平均年龄为21.7岁。每位患者均有大头和身材矮小的症状。95%的病例记录有脐疝,61%的病例记录有腹股沟疝。91%的患者有心脏病证据;这是最常见的死因。所有患者均频繁出现上呼吸道或下呼吸道感染。事实证明,中气道梗阻是一个特别的危险因素。注意到感觉神经性耳聋和不明原因视乳头水肿的发生率很高。强调了对这些患者进行定期医疗保健的重要性。