Severe to profound deafness may be associated with MYH9-related disease: report of 4 patients

MYH9-related disease (MYH9-RD) is a rare genetic syndromic disorder characterised by congenital thrombocytopenia and is associated with the risk of developing progressive sensorineural hearing loss, nephropathy and presenile cataracts during childhood or adult life. All consecutive patients enrolled...

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Bibliographic Details
Published in:Acta Otorhinolaryngol Ital
Main Authors: Canzi, P., Pecci, A., Manfrin, M., Rebecchi, E., Zaninetti, C., Bozzi, V., Benazzo, M.
Format: Artigo
Language:Inglês
Published: Pacini Editore SRL 2016
Subjects:
Audiology
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5225798/
https://ncbi.nlm.nih.gov/pubmed/27958602
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14639/0392-100X-702
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