Literature DB >> 6782888

The otologic manifestations of mucopolysaccharidoses.

E Hayes, R Babin, C Platz.   

Abstract

Patients with mucopolysaccharidoses are frequently hard of hearing. This disorder is often conductive in nature and considered the result of chronic serous otitis media. Such patients frequently undergo myringotomy. A coexisting progressive neurosensory hearing loss in some children is recognized far less often. Examination of temporal bones in such patients suggests arrested development including incomplete pneumatization. Hair cell dysfunction is implicated in the neurosensory component. Close communication among pediatrician, otolaryngologist, and speech and hearing personnel is essential to maximize the communicative skills of these patients.

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Mesh:

Year:  1980        PMID: 6782888

Source DB:  PubMed          Journal:  Am J Otol        ISSN: 0192-9763


  3 in total

1.  Hearing loss in patients with mucopolysaccharidosis II: data from HOS - the Hunter Outcome Survey.

Authors:  Annerose Keilmann; Todsaporn Nakarat; Iain A Bruce; David Molter; Gunilla Malm
Journal:  J Inherit Metab Dis       Date:  2011-08-25       Impact factor: 4.982

Review 2.  Neurological findings in Hunter disease: pathology and possible therapeutic effects reviewed.

Authors:  S Al Sawaf; E Mayatepek; B Hoffmann
Journal:  J Inherit Metab Dis       Date:  2008-07-13       Impact factor: 4.982

3.  The impact of laronidase treatment in otolaryngological manifestations of patients with mucopolysaccharidosis.

Authors:  Ana Paula Fiuza Funicello Dualibi; Ana Maria Martins; Gustavo Antônio Moreira; Marisa Frasson de Azevedo; Reginaldo Raimundo Fujita; Shirley Shizue Nagata Pignatari
Journal:  Braz J Otorhinolaryngol       Date:  2015-12-17
  3 in total

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