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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
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 |