Trucco Federica, Pedemonte Marina, Fiorillo Chiara, Tacchetti Paola, Brisca Giacomo, Bruno Claudio, Minetti Carlo
Pediatric Neurology and Muscle Disease Unit, Istituto Giannina Gaslini, Genova, Italy.
Pediatric Neurology and Muscle Disease Unit, Istituto Giannina Gaslini, Genova, Italy.
Respir Med. 2016 Oct;119:78-80. doi: 10.1016/j.rmed.2016.08.014. Epub 2016 Aug 22.
Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant inherited disorder characterized by selective weakness of face and upper arms and girdle. Respiratory involvement in FSHD has been described mainly in the most severely affected patients. In this work we tested the respiratory function by spirometry in 12 patients affected by FSHD with onset before 18 years. Spirometry results were correlated with motor involvement and compared to aged matched group of Becker patients. Of note FSHD patients present a peculiar pattern characterized by a flat shape in flow-volume loop. Respiratory volumes correlate with clinical severity and expiratory phase is specifically affected in comparison to other muscular dystrophies.
面肩肱型肌营养不良症(FSHD)是一种常染色体显性遗传性疾病,其特征为面部、上臂和肩胛带出现选择性肌无力。FSHD患者的呼吸功能受累主要在病情最严重的患者中有所描述。在这项研究中,我们对12例18岁前发病的FSHD患者进行了肺活量测定以检测其呼吸功能。肺活量测定结果与运动功能受累情况相关,并与年龄匹配的贝克型患者组进行了比较。值得注意的是,FSHD患者呈现出一种独特的模式,其流量-容积环呈扁平状。呼吸容积与临床严重程度相关,与其他肌营养不良症相比,呼气期受到的影响尤为明显。