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