Landau-Kleffner syndrome and central auditory disorders in children [electronic resource] / Makiko Kaga, Kimitaka Kaga.
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...
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Format: | Electronic eBook |
Language: | English |
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Singapore :
Springer,
2021.
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Series: | Modern otology and neurotology.
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245 | 1 | 0 | |a Landau-Kleffner syndrome and central auditory disorders in children |h [electronic resource] / |c Makiko Kaga, Kimitaka Kaga. |
260 | |a Singapore : |b Springer, |c 2021. | ||
300 | |a 1 online resource (146 pages) | ||
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490 | 1 | |a Modern Otology and Neurotology. | |
500 | |a Description based upon print version of record. | ||
505 | 0 | |a Intro -- Preface -- Contents -- Chapter 1: Introduction -- References -- Part I: Landau-Kleffner Syndrome (LKS) -- Chapter 2: History of LKS and Its Epidemiology -- 2.1 History of LKS -- 2.2 Epidemiology -- References -- Chapter 3: Diagnostic Paradigms -- 3.1 Clinical Symptoms -- 3.1.1 Onset of the Disease -- 3.1.1.1 Auditory Verbal and Language Symptoms -- 3.1.1.2 Musical Abilities -- 3.1.2 LKS Patients' Subjective Awareness of Their Own Disease -- 3.1.3 Behavioral Dysfunctions -- 3.1.4 Family History -- 3.1.5 Physical and Neuropsychological Examinations. | |
505 | 8 | |a 3.1.6 Intellectual Ability or IQs (Intellectual Quotients) in LKS Patients -- 3.1.7 Epileptic Seizures -- 3.2 Electroencephalography (EEG) -- 3.3 Audiometric Findings in LKS Patients -- 3.4 Evoked Responses in LKS Patients -- 3.4.1 Auditory Brainstem Responses (ABR) -- 3.4.2 Slow Vertex Responses (SVR) -- 3.4.3 Combined Evoked Potentials (EPs) and Event-Related Responses (ERPs) in LKS Patients -- 3.5 Event-Related Potentials -- 3.5.1 Mismatched Negativity (MMN) -- 3.5.2 The P300 Evoked Potential -- 3.6 Blood Exams, Urinalysis, and CSF Measures -- 3.7 Neuroimaging Examinations. | |
505 | 8 | |a 3.7.1 SPECT and PET Scan -- 3.8 Magnetoenechalography (MEG) -- References -- Chapter 4: Etiology and Genetics -- 4.1 Morphological Approach -- 4.1.1 Gross Anatomical Approach -- 4.1.2 Microscopic Approach -- 4.2 Present Status in Delineating the Etiology of LKS -- 4.2.1 LKS and Autism Spectrum Disorder (ASD) -- 4.2.1.1 Autistic Regression and Language Regression -- 4.3 Current Genetic Research -- References -- Chapter 5: Treatment and Long-Term Prognosis -- 5.1 Epilepsy -- 5.2 Surgical Interventions in the Treatment of LKS -- 5.3 Speech and Language Training -- References. | |
505 | 8 | |a Chapter 6: Case Histories -- 6.1 Patient A: 4 Years Old, Female -- 6.2 Patient B: 4 Years Old, Female -- 6.3 Patient C: 6 Years Old, Male -- 6.4 Patient D: 5 Years Old, Female -- 6.5 Patient E: 8 Years Old, Male -- 6.6 Patient F: 14 Years Old, Male -- 6.7 Patient G: 8 Years Old, Male -- 6.8 Patient H: 8 Years Old, Male -- 6.9 Patient I: 10 Years Old, Female -- Chapter 7: Fifty Years in the History of Landau-Kleffner Syndrome (LKS) -- Part II: Related Central Auditory Disorders -- Chapter 8: Adrenoleukodystrophy (ALD) -- 8.1 Etiology and Clinical Course of the Disease. | |
505 | 8 | |a 8.2 Clinical Types of ALD and Their Signs and Symptoms -- 8.3 Diagnosis of ALD -- 8.4 Hearing Impairment in ALD -- 8.5 Evaluation of Hearing in ALD -- 8.6 Case Reports of Japanese Patients with ALD and Auditory Agnosia (Furushima et al. 2015) -- 8.6.1 Case Histories of Three Patients -- 8.6.1.1 Patient 1 -- 8.6.1.2 Patient 2 -- 8.6.1.3 Patient 3 -- 8.6.2 MRIs of the Above Patients -- 8.6.2.1 Patient 1 (Fig. 8.4a) -- 8.6.2.2 Patient 2 (Fig. 8.4b) -- 8.6.2.3 Patient 3 (Fig. 8.4c) -- 8.6.3 Audiograms -- 8.6.4 ABR Findings -- 8.6.5 SVR and MMN -- 8.7 Summary -- 8.7.1 Hearing Impairment. | |
500 | |a 8.7.2 Auditory and Other Symptoms Caused by Localized Brain Lesions in Patients with ALD. | ||
504 | |a Includes bibliographical references. | ||
520 | |a 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. | ||
650 | 0 | |a Hearing disorders in children. |0 http://id.loc.gov/authorities/subjects/sh85059623. | |
650 | 0 | |a Hearing disorders in children |x Diagnosis. |0 http://id.loc.gov/authorities/subjects/sh85059624. | |
650 | 7 | |a Hearing disorders in children. |2 fast |0 (OCoLC)fst00953428. | |
650 | 7 | |a Hearing disorders in children |x Diagnosis. |2 fast |0 (OCoLC)fst00953430. | |
700 | 1 | |a Kaga, Kimitaka, |d 1944- |0 http://id.loc.gov/authorities/names/no2001097415 |1 http://isni.org/isni/000000007880363X. | |
776 | 0 | 8 | |i Print version: |a Kaga, Makiko |t Landau-Kleffner Syndrome and Central Auditory Disorders in Children |d Singapore : Springer Singapore Pte. Limited,c2021 |z 9789811014789. |
830 | 0 | |a Modern otology and neurotology. |0 http://id.loc.gov/authorities/names/no2014053215. | |
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