Myotonic Dystrophy

Disease Mechanism, Current Management and Therapeutic Development

Masanori P. Takahashi, Tsuyoshi Matsumura (Herausgeber)

Buch | Softcover

214 Seiten

2018 | Softcover reprint of the original 1st ed. 2018
Springer Verlag, Singapore
978-981-13-4436-7 (ISBN)

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This book provides an essential overview combining both clinical and fundamental research advances in myotonic dystrophy. The pathomechanism of myotonic dystrophy has long been unclear, but in the past decade, our understanding has shifted to a novel disease mechanism concept: “RNA disease”. Parallel to these advances in elucidating the pathophysiology, translational research is also progressing rapidly. The current challenge lies in assessing the effectiveness of treatment, and as such, there is a growing interest in observational studies of the disease’s various clinical symptoms.

The book introduces readers to the molecular mechanisms within each organ and the resultant clinical features, which are presented together. In particular, it focuses on the central nervous system, since the pathology of the brain (central nervous system manifestation) has rarely been addressed systematically and will pose a persistent challenge, even if therapies have greatly advanced in the future. In addition, the book addresses the latest developments, such as research using patient-derived iPS cells and therapeutic research.

Myotonic Dystrophy provides essential information for neurologists and researchers with an interest in muscle disease, including muscular dystrophy. Furthermore, since the disease involves various complications of the brain, heart, metabolism, etc., the book will be of great value to clinicians and researchers in the cardiovascular sciences, endocrinology, diabetes, dementia, and neuropsychology, as well as genetic specialists.

Masanori P. Takahashi, M.D., Ph.D. Department of Functional Diagnostic Science, Osaka University Graduate School of Medicine, Japan Tsuyoshi Matsumura, M.D., Ph.D. Department of Neurology, National Hospital Organization Toneyama National Hospital, Japan

Genetics of myotonic dystrophy (including cDM and DM2).- Basic Molecular pathomechanism.- Clinical features in skeletal muscle and their underlying molecular mechanism.- Clinical features in heart and their underlying molecular mechanism.- Clinical features of central nervous system.- Pathological changes in DM brain.- Molecular defect in DM central nervous system.- Respiratory feature in DM.- Glucose intolerance in DM.- Lipid metabolism in DM.- Dysphagia in DM.- DM patient-derived iPS cells.- Therapeutic development in DM.

Erscheint lt. Verlag	29.12.2018
Zusatzinfo	42 Illustrations, color; 16 Illustrations, black and white; VIII, 214 p. 58 illus., 42 illus. in color.
Verlagsort	Singapore
Sprache	englisch
Maße	155 x 235 mm
Themenwelt	Medizinische Fachgebiete ► Innere Medizin ► Kardiologie / Angiologie
	Medizin / Pharmazie ► Medizinische Fachgebiete ► Neurologie
	Studium ► 1. Studienabschnitt (Vorklinik) ► Biochemie / Molekularbiologie
Schlagworte	CNBP • DM • DMPK • Hereditary Disease • Muscle weakness • myotonic dystrophy • RNA disease
ISBN-10	981-13-4436-1 / 9811344361
ISBN-13	978-981-13-4436-7 / 9789811344367
Zustand	Neuware