Total hip arthroplasty in Hurler syndrome - 8 years follow up - A case report with review of literature

被引：2
作者：
Gautam, Deepak [1 ]
Malhotra, Rajesh [1 ]
机构：
[1] All India Inst Med Sci, Dept Orthoped, New Delhi 110029, India
来源：
JOURNAL OF ORTHOPAEDICS | 2018年 / 15卷 / 01期
基金：
英国惠康基金;
关键词：
Mucopolysaccharidosis; Hurler syndrome; Total hip arthroplasty;
D O I：
10.1016/j.jor.2018.01.036
中图分类号：
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学（修复外科学）];
学科分类号：
摘要：
Life expectancy in Hurler syndrome is significantly improved by enzyme therapy with bone marrow transplantation. However, the deterioration of skeletal abnormalities persists. Hip dysplasia is a common presentation which may progress to significant hip arthritis requiring total hip arthroplasty at later stage. We report a long-term outcome of cementless total hip arthroplasty in a patient with Hurler syndrome who was successfully treated with bone marrow transplant.
引用
收藏
页码：111 / 113
页数：3
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