Kartagener`s Syndrome: A Case Report.

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dc.contributor.authorPonnathpur, Lakshmi
dc.contributor.authorShantharam, Lakshmi
dc.date.accessioned2017-01-24T09:25:47Z
dc.date.available2017-01-24T09:25:47Z
dc.date.issued2013-07
dc.description.abstractKartagener`s syndrome, a rare autosomal recessive disorder is a type of primary ciliary dyskinesia (PCD) associated situs inversus, bronchiectasis, sinusitis and male infertility. We present a case of a 12-year-old boy who came with features of bilateral glue ear, recurrent sinusitis, adenotonsillitis, obstructive sleep apnea and situ inversus. He was diagnosed to have Kartagener`s syndrome and was treated with bilateral grommet insertion, bilateral antral lavage and adenotonsillectomy to alleviate his symptoms.en_US
dc.identifier.citationPonnathpur Lakshmi, Shantharam Lakshmi. Kartagener`s Syndrome: A Case Report. Indian Journal of Clinical Practice. 2013 July; 24(2): 149-151.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/182356
dc.language.isoenen_US
dc.source.urihttps://medind.nic.in/iaa/t13/i7/iaat13i7p149.pdfen_US
dc.subjectKartagener`s syndromeen_US
dc.subjectsitus inversusen_US
dc.subjectprimary ciliary dyskinesiaen_US
dc.titleKartagener`s Syndrome: A Case Report.en_US
dc.typeArticleen_US
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