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Landau-Kleffner syndrome and central...
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Kaga, Makiko.
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Landau-Kleffner syndrome and central auditory disorders in children
Record Type:
Electronic resources : Monograph/item
Title/Author:
Landau-Kleffner syndrome and central auditory disorders in children/ by Makiko Kaga, Kimitaka Kaga.
Author:
Kaga, Makiko.
other author:
Kaga, Kimitaka.
Published:
Singapore :Springer Singapore : : 2021.,
Description:
x, 144 p. :ill., digital ;24 cm.
[NT 15003449]:
1. Introduction -- Part I. Landau-Kleffner syndrome (LKS) -- 2. History of LKS and epidemiology -- 3. Diagnostic Paradigms -- 4. Etiology and Genetics -- 5. Treatment and Long Term Prognosis -- 6. Case histories. -7. Fifty years of Landau-Kleffner Syndrome. Part II. Related Central Auditory Disorders -- 8. Adrenoleukodystrophy -- 9. Cerebrovascular accidents -- 10. Auditory agnosia in children after Herpes Encephalitis -- 11. Transient auditory agnosia /cortical deafness during the recovery phase of acute encephalopathy of unknown origin. -12. Pelizaeus-Merzbacher Disease. -13. Long-term hydrocephalus. -14. Brain malformation and hydrocephalus.
Contained By:
Springer Nature eBook
Subject:
Hearing disorders in children. -
Online resource:
https://doi.org/10.1007/978-981-10-1479-6
ISBN:
9789811014796
Landau-Kleffner syndrome and central auditory disorders in children
Kaga, Makiko.
Landau-Kleffner syndrome and central auditory disorders in children
[electronic resource] /by Makiko Kaga, Kimitaka Kaga. - Singapore :Springer Singapore :2021. - x, 144 p. :ill., digital ;24 cm. - Modern otology and neurotology,2567-2169. - Modern otology and neurotology..
1. Introduction -- Part I. Landau-Kleffner syndrome (LKS) -- 2. History of LKS and epidemiology -- 3. Diagnostic Paradigms -- 4. Etiology and Genetics -- 5. Treatment and Long Term Prognosis -- 6. Case histories. -7. Fifty years of Landau-Kleffner Syndrome. Part II. Related Central Auditory Disorders -- 8. Adrenoleukodystrophy -- 9. Cerebrovascular accidents -- 10. Auditory agnosia in children after Herpes Encephalitis -- 11. Transient auditory agnosia /cortical deafness during the recovery phase of acute encephalopathy of unknown origin. -12. Pelizaeus-Merzbacher Disease. -13. Long-term hydrocephalus. -14. Brain malformation and hydrocephalus.
This book addresses current topics concerning Landau-Kleffner Syndrome (LKS) and related central auditory disorders from the perspectives of epidemiology, diagnosis, genetics and clinical treatment. LKS is a rare childhood neurological disorder and manifests auditory agnosia as the central auditory verbal dysfunction. In many cases, LKS patients also suffer from epileptic seizures. The book is divided into two parts, the first of which outlines LKS from its historical background to clinical treatment. In turn, the second part examines current topics involving related central auditory disorders, for purposes of comparing them with LKS. The book offers a valuable resource for many specialists, such as pediatric neurologists, neuropsychologists, audiologists and epileptologists, with an interest in this field.
ISBN: 9789811014796
Standard No.: 10.1007/978-981-10-1479-6doiSubjects--Topical Terms:
636956
Hearing disorders in children.
LC Class. No.: RF291.5.C45 / K34 2021
Dewey Class. No.: 618.920978
Landau-Kleffner syndrome and central auditory disorders in children
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1. Introduction -- Part I. Landau-Kleffner syndrome (LKS) -- 2. History of LKS and epidemiology -- 3. Diagnostic Paradigms -- 4. Etiology and Genetics -- 5. Treatment and Long Term Prognosis -- 6. Case histories. -7. Fifty years of Landau-Kleffner Syndrome. Part II. Related Central Auditory Disorders -- 8. Adrenoleukodystrophy -- 9. Cerebrovascular accidents -- 10. Auditory agnosia in children after Herpes Encephalitis -- 11. Transient auditory agnosia /cortical deafness during the recovery phase of acute encephalopathy of unknown origin. -12. Pelizaeus-Merzbacher Disease. -13. Long-term hydrocephalus. -14. Brain malformation and hydrocephalus.
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This book addresses current topics concerning Landau-Kleffner Syndrome (LKS) and related central auditory disorders from the perspectives of epidemiology, diagnosis, genetics and clinical treatment. LKS is a rare childhood neurological disorder and manifests auditory agnosia as the central auditory verbal dysfunction. In many cases, LKS patients also suffer from epileptic seizures. The book is divided into two parts, the first of which outlines LKS from its historical background to clinical treatment. In turn, the second part examines current topics involving related central auditory disorders, for purposes of comparing them with LKS. The book offers a valuable resource for many specialists, such as pediatric neurologists, neuropsychologists, audiologists and epileptologists, with an interest in this field.
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based on 0 review(s)
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EB RF291.5.C45 K34 2021
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