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Progress in the diagnosis and treatment of Kartagener syndrome in children / 国际儿科学杂志
International Journal of Pediatrics ; (6): 937-940, 2018.
Artigo em Chinês | WPRIM | ID: wpr-732695
ABSTRACT
Kartagener syndrome is a rare autosomal recessive disease with low incidence.Clinically,typical visceral inversion,bronchiectasis and sinusitis triad are typical.The pathogenesis of the disease is not clear.The principle of treatment is mainly symptomatic treatment,postponing the progress of bronchiectasis,Lack of fundamental treatment.The disease generally has a good prognosis.This article reviews recent advances in the diagnosis and treatment of Kartagener syndrome at home and abroad.

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Tipo de estudo: Estudo diagnóstico Idioma: Chinês Revista: International Journal of Pediatrics Ano de publicação: 2018 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Tipo de estudo: Estudo diagnóstico Idioma: Chinês Revista: International Journal of Pediatrics Ano de publicação: 2018 Tipo de documento: Artigo