Early-onset facioscapulohumeral muscular dystrophy with Coats syndrome: a case report / 中华神经科杂志
Chinese Journal of Neurology
; (12): 46-48, 2019.
Article
in Zh
| WPRIM
| ID: wpr-734888
Responsible library:
WPRO
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.
Full text:
1
Database:
WPRIM
Language:
Zh
Journal:
Chinese Journal of Neurology
Year:
2019
Document type:
Article