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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.
Key words
Full text: 1 Database: WPRIM Language: Zh Journal: Chinese Journal of Neurology Year: 2019 Document type: Article
Full text: 1 Database: WPRIM Language: Zh Journal: Chinese Journal of Neurology Year: 2019 Document type: Article