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.
Artículo
en Chino
| 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:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Tipo de estudio:
Estudio diagnóstico
Idioma:
Chino
Revista:
International Journal of Pediatrics
Año:
2018
Tipo del documento:
Artículo
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