Abstract
We herein present a patient with auditory agnosia that may provide insight into this condition.
This patient was a 27-year-old female. She was diagnosed with congenital spina bifida and had experienced CSF leakage since birth. Brain CT revealed hydrocephalus immediately after birth and at 4 months of age she underwent her first ventriculoperitoneal (VP) shunt surgery. She lost all hearing in her right ear immediately after surgery and she began to rapidly lose hearing in her left ear about 25 months after the onset of her right ear problems. However, ABRs from both ears were normal.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Guyton AC, Hall JE. Textbook of medical physiology. 10th ed. Philadelphia: WB Saunders; 2000. p. 608–9.
Ironside JW, Pickard JD. Raised intracranial pressure, oedema and hydrocephalus. In: Graham DJ, Lantos PL, editors. Greenfield’s neuropathology. 7th ed. London: Arnold; 2002. p. 193–231.
Shivashankar N, Shashikala HR, Nagaraja D, et al. Pure word deafness in two patients with subcortical lesions. Clin Neurol Neurosurg. 2001;103:201–5.
Zhang Q, Kaga K, Hayashi A. Auditory agnosia due to long-term severe hydrocephalus caused by spina bifida—specific auditory pathway versus nonspecific auditory pathway. Acta Otolaryngol. 2011;131:787–92.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
Copyright information
© 2021 Springer Science+Business Media Singapore
About this chapter
Cite this chapter
Kaga, K. (2021). Long-Term Hydrocephalus. In: Landau-Kleffner Syndrome and Central Auditory Disorders in Children. Modern Otology and Neurotology. Springer, Singapore. https://doi.org/10.1007/978-981-10-1479-6_13
Download citation
DOI: https://doi.org/10.1007/978-981-10-1479-6_13
Published:
Publisher Name: Springer, Singapore
Print ISBN: 978-981-10-1478-9
Online ISBN: 978-981-10-1479-6
eBook Packages: MedicineMedicine (R0)