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Gene Mutations in Primary Ciliary Dyskinesia Related to Otitis Media

Gene Mutations in Primary Ciliary Dyskinesia Related to Otitis Media

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1492705133

Gene Mutations in Primary Ciliary Dyskinesia Related to Otitis Media

About this item

Full title

Gene Mutations in Primary Ciliary Dyskinesia Related to Otitis Media

Publisher

Boston: Springer US

Journal title

Current allergy and asthma reports, 2014-03, Vol.14 (3), p.420-420, Article 420

Language

English

Formats

Publication information

Publisher

Boston: Springer US

More information

Scope and Contents

Contents

Otitis media with effusion (OME) is the most common cause of conductive hearing loss in children and is strongly associated with primary ciliary dyskinesia (PCD). Approximately half of the children with PCD require otolaryngology care, posing a major problem in this population. Early diagnosis of PCD is critical in these patients to minimise the co...

Alternative Titles

Full title

Gene Mutations in Primary Ciliary Dyskinesia Related to Otitis Media

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_1492705133

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1492705133

Other Identifiers

ISSN

1529-7322

E-ISSN

1534-6315

DOI

10.1007/s11882-014-0420-1

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