Objective: Incomplete partition type 3 (IP3) malformation deafness is a rare hereditary cause of congenital or rapid progressive hearing loss. The children present with a severe to profound mixed hearing loss and temporal bone imaging show a typical inner ear malformation classified as IP3. Cochlear implantation is one option of hearing restoration in severe cases. Little is known about other specific difficulties these children might exhibit, for instance possible neurodevelopmental symptoms. Material and methods: Ten 2; 0 to 9; 6-year-old children with IP3 malformation deafness (nine boys and one girl) with cochlear implants were evaluated with a retrospective chart review in combination with an additional extensive multidisciplinary asse...
Objectives: This multicenter study evaluated the auditory performance and speech production outcomes...
Objectives: Evaluating the value of MRI for assessing congenital anomalies of the inner ear in child...
The present study aims are to clarify causes of congenital hearing loss in children who received coc...
Objective: Incomplete partition type 3 (IP3) malformation deafness is a rare hereditary cause of con...
Objective: To evaluate if cochlear implantation is safe and constitutes an option for hearing rehabi...
Aims. This study is aimed at (1) analyzing the clinical manifestations and genetic features of a nov...
Copyright © 2015 Micol Busi et al. This is an open access article distributed under the Creative Com...
PURPOSE: The authors report on a 7-year-old male, designated FR, who has severe sensorineural hearin...
Background. Specific clinical conditions could compromise cochlear implantation outcomes and drastic...
Cochlear implantation is currently the treatment of choice for children with severe to profound hear...
hearing loss is one of the most common disabilities and has lifelong consequences for affected child...
Objectives: CHARGE syndrome is a complex cluster of congenital abnormalities, these children may hav...
Objective: To investigate the roles of genetic diagnosis and imaging studies, as well as other progn...
Objective: While investigators have reported that patients with GJB2-associated deafness and cochlea...
PURPOSE:X-linked deafness (XLD) is a rare disease, characterized by typical cochlear incomplete part...
Objectives: This multicenter study evaluated the auditory performance and speech production outcomes...
Objectives: Evaluating the value of MRI for assessing congenital anomalies of the inner ear in child...
The present study aims are to clarify causes of congenital hearing loss in children who received coc...
Objective: Incomplete partition type 3 (IP3) malformation deafness is a rare hereditary cause of con...
Objective: To evaluate if cochlear implantation is safe and constitutes an option for hearing rehabi...
Aims. This study is aimed at (1) analyzing the clinical manifestations and genetic features of a nov...
Copyright © 2015 Micol Busi et al. This is an open access article distributed under the Creative Com...
PURPOSE: The authors report on a 7-year-old male, designated FR, who has severe sensorineural hearin...
Background. Specific clinical conditions could compromise cochlear implantation outcomes and drastic...
Cochlear implantation is currently the treatment of choice for children with severe to profound hear...
hearing loss is one of the most common disabilities and has lifelong consequences for affected child...
Objectives: CHARGE syndrome is a complex cluster of congenital abnormalities, these children may hav...
Objective: To investigate the roles of genetic diagnosis and imaging studies, as well as other progn...
Objective: While investigators have reported that patients with GJB2-associated deafness and cochlea...
PURPOSE:X-linked deafness (XLD) is a rare disease, characterized by typical cochlear incomplete part...
Objectives: This multicenter study evaluated the auditory performance and speech production outcomes...
Objectives: Evaluating the value of MRI for assessing congenital anomalies of the inner ear in child...
The present study aims are to clarify causes of congenital hearing loss in children who received coc...