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

Canzi, P; Pecci, A; Manfrin, M; Rebecchi, E; Zaninetti, C; Bozzi, V; Benazzo, M

Canzi, P; Pecci, A; Manfrin, M; Rebecchi, E; Zaninetti, C; Bozzi, V; Benazzo, M.

Affiliation

Canzi P; Department of Otorhinolaryngology, IRCCS Policlinico San Matteo Foundation and University of Pavia, Italy.
Pecci A; Department of Internal Medicine, IRCCS Policlinico San Matteo Foundation and University of Pavia, Italy.
Manfrin M; Department of Otorhinolaryngology, IRCCS Policlinico San Matteo Foundation and University of Pavia, Italy.
Rebecchi E; Department of Otorhinolaryngology, IRCCS Policlinico San Matteo Foundation and University of Pavia, Italy.
Zaninetti C; Department of Internal Medicine, IRCCS Policlinico San Matteo Foundation and University of Pavia, Italy.
Bozzi V; Department of Internal Medicine, IRCCS Policlinico San Matteo Foundation and University of Pavia, Italy.
Benazzo M; Department of Otorhinolaryngology, IRCCS Policlinico San Matteo Foundation and University of Pavia, Italy.

Acta Otorhinolaryngol Ital ; 36(5): 415-420, 2016 Oct.

Article in En | MEDLINE | ID: mdl-27958602

Subject(s)

Deafness/etiology; Hearing Loss, Sensorineural/complications; Thrombocytopenia/congenital; Adult; Deafness/diagnosis; Female; Humans; Male; Retrospective Studies; Severity of Illness Index; Thrombocytopenia/complications

Key words

Genetic syndrome; Hearing loss; MYH9

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thrombocytopenia / Deafness / Hearing Loss, Sensorineural Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male Language: En Journal: Acta Otorhinolaryngol Ital Year: 2016 Document type: Article Affiliation country: Italy Country of publication: Italy

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