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.
Artigo
em Chinês
| 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.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Idioma:
Chinês
Revista:
Chinese Journal of Neurology
Ano de publicação:
2019
Tipo de documento:
Artigo
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