OBJECTIVE: Description of two siblings with unexplained, progressive, perceptive hearing loss after head trauma. DESIGN: Case report. SUBJECTS: Two siblings aged six and eight years old with bilateral, intermittent but progressive hearing loss. RESULTS: These patients had a c.1172G>A (p.Ser391Asn) mutation in the SLC26A4 gene, which has not previously been reported and which caused Pendred or enlarged vestibular aqueduct syndrome. The diagnosis was based on the perceptive hearing loss, computed tomography findings and mutation analysis. The patients were each fitted with a cochlear implant because of their severe, progressive, perceptive hearing loss with deep fluctuations. The results were good. CONCLUSION: Further testing for the presence...
Following systematic skull imaging of hundred and sixty seven individuals attending a medical referr...
Individual’s hearing performance after cochlear implant (CI) is variable and depends on different fa...
SummaryAimrecent progresses in molecular biology have been made in the diagnosis of sensorineural he...
A 4-month-old baby girl whose parents and 6-year-old brother have severe-to-profound sensorineural h...
hearing loss is one of the most common disabilities and has lifelong consequences for affected child...
Objective: Incomplete partition type 3 (IP3) malformation deafness is a rare hereditary cause of con...
Objective: To characterize the clinical findings in a patient with hearing loss harboring an A8296G ...
The present study aims are to clarify causes of congenital hearing loss in children who received coc...
Objective: To evaluate the long-term ipsi- and contralateral hearing of patients with a unilateral e...
OBJECTIVES/HYPOTHESIS: To describe the clinical experience and characterize the outcomes of cochlear...
Introduction: Alström Syndrome is a rare disease caused by mutations in ALMS1 gene. It is characteri...
Introduction: Vestibular aqueducts follow a route through the inner ear that terminates within the s...
With prevalence figures close to 0.2% at birth and rising to 0.35% during adolescence, hearing loss ...
Summary: Hearing loss is a multifaceted condition with many etiologies, among which genetic mutation...
OBJECTIVES: Mutations in the SLC26A4 gene (7q22.3-7q31.1) are considered one of the most common caus...
Following systematic skull imaging of hundred and sixty seven individuals attending a medical referr...
Individual’s hearing performance after cochlear implant (CI) is variable and depends on different fa...
SummaryAimrecent progresses in molecular biology have been made in the diagnosis of sensorineural he...
A 4-month-old baby girl whose parents and 6-year-old brother have severe-to-profound sensorineural h...
hearing loss is one of the most common disabilities and has lifelong consequences for affected child...
Objective: Incomplete partition type 3 (IP3) malformation deafness is a rare hereditary cause of con...
Objective: To characterize the clinical findings in a patient with hearing loss harboring an A8296G ...
The present study aims are to clarify causes of congenital hearing loss in children who received coc...
Objective: To evaluate the long-term ipsi- and contralateral hearing of patients with a unilateral e...
OBJECTIVES/HYPOTHESIS: To describe the clinical experience and characterize the outcomes of cochlear...
Introduction: Alström Syndrome is a rare disease caused by mutations in ALMS1 gene. It is characteri...
Introduction: Vestibular aqueducts follow a route through the inner ear that terminates within the s...
With prevalence figures close to 0.2% at birth and rising to 0.35% during adolescence, hearing loss ...
Summary: Hearing loss is a multifaceted condition with many etiologies, among which genetic mutation...
OBJECTIVES: Mutations in the SLC26A4 gene (7q22.3-7q31.1) are considered one of the most common caus...
Following systematic skull imaging of hundred and sixty seven individuals attending a medical referr...
Individual’s hearing performance after cochlear implant (CI) is variable and depends on different fa...
SummaryAimrecent progresses in molecular biology have been made in the diagnosis of sensorineural he...