Shapiro J, Strome M, Crocker A C
Ann Otol Rhinol Laryngol. 1985 Sep-Oct;94(5 Pt 1):458-61. doi: 10.1177/000348948509400508.
The Hurler and Hunter syndromes are two forms of mucopolysaccharidosis. Although the diseases are rare, those afflicted commonly require otolaryngologic consultation. Upper airway obstruction is often severe, progressive, and not infrequently the suspected cause of death in these patients. Four patients with these problems are presented. In all of the children, obstructive sleep apnea was a major management problem. This and other upper airway difficulties are detailed with clinical and pathological correlates.
黏多糖贮积症Ⅰ型(Hurler综合征)和黏多糖贮积症Ⅱ型(Hunter综合征)是黏多糖贮积症的两种类型。尽管这些疾病很罕见,但患者通常需要耳鼻喉科会诊。上气道梗阻往往严重、呈进行性发展,并且在这些患者中常常是疑似死因。本文介绍了4例有这些问题的患者。在所有这些儿童中,阻塞性睡眠呼吸暂停是一个主要的治疗难题。现将这一情况及其他上气道问题结合临床和病理联系进行详细阐述。