Kartagener’s syndrome: review of a case series

BACKGROUND: Kartagener Syndrome (KS) is a rare autosomal recessive genetic disorder, resulting in a group of clinical manifestations, including bronchiectasis, chronic pansinusitis and situs inversus. METHODS: We hereby reviewed eight cases of this rare entity selected from patients attending our ou...

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Detalles Bibliográficos
Autores principales: Ciancio, Nicola, de Santi, Maria Margherita, Campisi, Raffaele, Amato, Laura, Di Martino, Giuseppina, Di Maria, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4465165/
https://www.ncbi.nlm.nih.gov/pubmed/26075070
http://dx.doi.org/10.1186/s40248-015-0015-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4465165/
https://www.ncbi.nlm.nih.gov/pubmed/26075070
http://dx.doi.org/10.1186/s40248-015-0015-2

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