This practical book describes only neurometabolic hereditary diseases for which treatment is available and encourages the general neurologist to think of the most common neurometabolic hereditary diseases, which they might have encounteredand never considered in the differential diagnosis. The book provides information on how to deal with diseases that require special therapy such as enzymatic replacement therapy in Fabry disease and Pompe disease. In addition, it discusses diseases that are not easily recognized (i.e. Niemann-Pick disease type C), and diseases with clinical features mimicking other common neurodegenerative diseases (i.e. Wilson's disease).
Neurometabolic Hereditary Diseases is written with a clinical focus for adult neurologists working in general hospitals.
- ISBN: 978-3-319-76146-6
- Editorial: Springer
- Encuadernacion: Cartoné
- Páginas: 150
- Fecha Publicación: 12/07/2018
- Nº Volúmenes: 1
- Idioma: Inglés