Etiological diagnosis in the hearing impaired newborn: proposal of a flow chart |
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Authors: | De Leenheer E M R Janssens S Padalko E Loose D Leroy B P Dhooge I J |
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Institution: | a Department of Otorhinolaryngology and Head & Neck Surgery, Ghent University Hospital & Ghent University, 1P1, UZGhent, De Pintelaan 185, 9000 Ghent, Belgium b Department of Medical Genetics, Ghent University Hospital, Ghent, Belgium c Department of Clinical Chemistry, Microbiology and Immunology Virology, Ghent University Hospital, Ghent, Belgium d Department of Otorhinolaryngology and Head & Neck Surgery, Ghent University Hospital, Ghent, Belgium e Department of Ophthalmology & Ctr for Medical Genetics, Ghent University Hospital & Ghent University, Ghent, Belgium |
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Abstract: | ObjectiveMost industrialized countries have introduced some form of universal newborn hearing screening program. Both identification and rehabilitation of hearing loss in newborns have evolved to an acceptable standard and the need for a standardized etiological protocol is emerging.MethodsExtensive literature search to determine which investigations can help identifying the cause of congenital hearing loss and how to limit extensive testing in these children by taking into account the most prevalent causes.FindingsA stepwise approach to detect the cause of hearing loss in children with congenital sensorineural hearing loss was developed.ConclusionIn general it is advised to first rule out Cx26/Cx30 and infectious causes (cytomegalovirus and, if indicated, toxoplasmosis and rubella), and to preserve more extensive investigations for those children in whom these causes do not explain the hearing loss. |
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Keywords: | Congenital Newborn Hearing loss Deafness Etiology |
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