1.
Chinese Journal of Neurology
;
(12): 46-48, 2019.
Article
in Chinese
| WPRIM
| ID: wpr-734888
ABSTRACT
Early-onset facioscapulohumeral muscular dystrophy is a rare clinical syndrome characterized by severe muscle weakness started in early childhood,with extramuscular manifestations such as retinal vascular tortuosity,sensorineural hearing loss and epilepsy.Herein we report a case with early-onset facioscapulohumeral muscular dystrophy and Coats syndrome.Early diagnosis of Coats syndrome is critical for the prognosis.