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Otologic features in children with primary ciliary dyskinesia.: Otologic features in children with PCD

Virginie Prulière-Escabasse 1, * André Coste 1 Pierre Chauvin 2 Brigitte Fauroux 3, 4 Aline Tamalet 3, 4 Erea-Noel Garabedian 5 Estelle Escudier 6 Gilles Roger 5
* Corresponding author
1 INSERM U955, équipe 13
Service d'ORL et de chirurgie cervico-faciale, IMRB - Institut Mondor de Recherche Biomédicale
2 DS3 - ESIM - Déterminants Sociaux de la Santé et du Recours aux Soins
3 Service de pneumologie [CHU Trousseau]
4 CR Saint-Antoine - Centre de Recherche Saint-Antoine
5 Service d'ORL pédiatrique et Chirurgie Cervico-faciale [CHU Trousseau]
6 INSERM U955, équipe 13
Service de génétique et embryologie médicales [CHU Trousseau], Physiopathologie des maladies génétiques d'expression pédiatrique, IMRB - Institut Mondor de Recherche Biomédicale
Abstract : Despite continuous antibiotic therapy, the middle ear condition in PCD remained severe throughout childhood, with improvement only after age 18 years. Armstrong grommet placement did not improve the middle ear condition. Central complex defect is a marker of severity.
Keywords : cilia Kartagener syndrome serous otitis media conductive hearing loss
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https://www.hal.inserm.fr/inserm-00561338
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Submitted on : Thursday, November 3, 2011 - 9:36:17 AM
Last modification on : Wednesday, August 19, 2020 - 11:18:05 AM
Long-term archiving on: : Saturday, February 4, 2012 - 2:20:21 AM

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IMRB | U938 | DS3 | U707 | UPEC | UPEC-UPEM | UPMC | U933 | SORBONNE-UNIVERSITE | SU-MEDECINE

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Virginie Prulière-Escabasse, André Coste, Pierre Chauvin, Brigitte Fauroux, Aline Tamalet, et al.. Otologic features in children with primary ciliary dyskinesia.: Otologic features in children with PCD. Archives of Otolaryngology Head and Neck Surgery, American Medical Association, 2010, 136 (11), pp.1121-6. ⟨10.1001/archoto.2010.183⟩. ⟨inserm-00561338⟩

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