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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