Late-onset auditory deprivation or "inactivity" phenomenon has been reported in single cases only because it has not been possible to assemble a larger number of calculable cohorts for which all necessary details concerning individual histories are available. Subjects should not be older than 60 years of age and should have had asymmetric hearing for at least about 10 years or should have been wearers of monaurally fitted hearing aids. The development of late-onset auditory deprivation is presented in 6 single cases. All were assessed by the Freiburg speech discrimination test and the distorted Freiburg speech test, with the latter showing greater sensitivity and variability. It is of special interest that the quotient of distorted speech is reduced in subjects who have normal hearing in one ear and considerable hearing loss in the other ear (for example, in the case of unilateral microtia). This effect may be evidence for significant activation of hearing selectivity developing in the brainstem versus inactivation.
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Pathogens
November 2024
Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL 35233, USA.
Congenital cytomegalovirus infection (cCMV) is a frequent cause of non-hereditary sensorineural hearing loss (SNHL) and developmental disabilities. The contribution of cCMV to childhood hearing loss has been estimated to be about 25% of all hearing loss in children at 4 years of age. Although the vestibular insufficiency (VI) in cCMV has not been well-characterized and therefore, underestimated, recent studies suggest that VI is also frequent in children with cCMV and can lead to adverse neurodevelopmental outcomes.
View Article and Find Full Text PDFIndian J Otolaryngol Head Neck Surg
December 2024
All India Institute of Speech and Hearing, Naimisham campus, Manasagangothri, Mysore, 570006 India.
The study aimed to assess the risk of hearing loss in full-term neonates with hyperbilirubinemia, examining the relationship between bilirubin levels, onset age of hyperbilirubinemia, and hearing impairment. Additionally, it investigated whether hearing loss was transient or late-onset, using a cost-effective double-screening method. The study included 160 full-term neonates aged 0-1 month.
View Article and Find Full Text PDFCureus
October 2024
Psychiatry, Ng Teng Fong General Hospital, Singapore, SGP.
Alzheimers Res Ther
October 2024
Department of Psychiatry, Depression Center, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Neurologist
January 2025
Department of Neurology, University of Utah.
Introduction: The C9orf72 mutation can manifest in diverse clinical ways, including rapid cognitive decline, parkinsonism, or late-life neuropsychiatric symptoms, sometimes mimicking autoimmune encephalitis.
Case Report: A 64-year-old female presented to the autoimmune neurology clinic with rapidly progressive dementia (RPD) associated with episodes of headache, confusion, auditory hallucinations, and abnormal electroencephalogram. She was treated empirically at an outside hospital for possible autoimmune encephalitis with intravenous methylprednisolone, but there was no improvement, and rapid cognitive decline continued.
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