4.4 Article

Systemic manifestations and symptom burden of facioscapulohumeral muscular dystrophy in a referral cohort

期刊

MUSCLE & NERVE
卷 65, 期 4, 页码 415-421

出版社

WILEY
DOI: 10.1002/mus.27493

关键词

cardiac arrhythmias; facioscapulohumeral dystrophy; myopathy; respiratory insufficiency; systemic manifestations

向作者/读者索取更多资源

This study reviewed the medical records of 87 patients with facioscapulohumeral muscular dystrophy (FSHD) and found that besides muscle weakness, these patients also experienced pain, difficulty sleeping, headaches, and altered mood. Some patients also had complications such as sensorineural hearing loss, cardiac disease, dysphagia, and respiratory insufficiency. Further screening for these systemic manifestations is warranted.
Introduction/Aims The full spectrum of the clinical phenotype of facioscapulohumeral muscular dystrophy (FSHD), beyond skeletal muscle weakness, remains poorly characterized. In this study, we describe systemic manifestations and symptom burden in a large series of FSHD patients. Methods We performed a retrospective chart review of FSHD patients seen at our institution between 2000 and 2017. We reviewed patients' responses to a comprehensive review of symptoms and the results of diagnostic testing for sensorineural hearing loss, cardiac disease, dysphagia, ocular abnormalities, and respiratory insufficiency. We assessed the association between disease manifestations and age of onset, genetic profile, and disease duration. Results We identified 87 patients with FSHD. The most common reported symptoms included pain (71%), difficulty sleeping (41%), headaches (27%), and altered mood (24%). When tested, 7 of 16 (44%) patients had sensorineural hearing loss, 20 of 60 (33%) had cardiac arrhythmias or conduction defects, 17 of 45 (38%) had echocardiogram abnormalities, 12 of 25 (48%) had reduced forced vital capacity, and 4 of 10 (40%) had oropharyngeal dysphagia. However, patients with these abnormalities represented 8%, 23%, 20%, 14%, and 5% of total number of patients, respectively, as uniform screening was lacking. Ocular pathology attributable to FSHD was not detected. Discussion FSHD demonstrates a broad clinical phenotype. Increased vigilance among neurologists to screen for systemic manifestations of the disease is warranted. More uniform screening and future population-based studies are needed to compare findings in FSHD patients with the general population.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据