Buch, Englisch, 147 Seiten, Previously published in hardcover, Format (B × H): 178 mm x 254 mm, Gewicht: 343 g
Diagnosis and Case Study
Buch, Englisch, 147 Seiten, Previously published in hardcover, Format (B × H): 178 mm x 254 mm, Gewicht: 343 g
ISBN: 978-981-13-5075-7
Verlag: Springer Nature Singapore
This book provides up-to-date information on various inherited neurological disorders, presenting 40 cases of inherited neurological disorders with genetic diagnosis and/or pathological confirming. These disorders include cerebellar ataxia (SCA1, SCA2, SCA3, etc.), epileptic attacks related disorders (MELAS, MERRF, TSC, etc.), motor neuron related disorders (ALS, HSP, CMT, etc.), movement disorders (PD, PKD, DRD, etc.), ion channel diseases (hypokalemic periodic paralysis, normal potassium periodic paralysis), muscle diseases (DMD, FSHD, LSM, etc.), and dementia and psychiatric disorders (HD, CADASIL, CARASIL, etc.).
With the format of case study, one type of diseases is discussed on each chapter, basically consisted of 5 sections. Section 1 focuses on the detailed clinical features, physical examination and hematological examination, while Section 2 addresses questions regarding diagnosis and differential diagnosis. Additional information such as imaging material and genetic/pathological results are provided in Section 3, followed by the final diagnosis in Section 4. Section 5 presents a systemic review for each specific disease. The book will benefit clinicians especially neurologists, medical students, researchers and healthcare professionals facing difficult cases, particularly those involving fundamental research and diagnostic methods.
Zielgruppe
Professional/practitioner
Autoren/Hrsg.
Fachgebiete
Weitere Infos & Material
Cerebellar ataxia.- Epileptic attacks related disorders.- Motor neuron related disorders.- Movement disorders.- Ion channel diseases.- Muscle Diseases.- Dementia and psychiatric disorders.




