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 Printable version |
Orphan Drugs in Epilepsy
Orphan Drugs in Epilepsy
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Marina Nikanorova, Pierre Genton, Svein Johannessen
2011
Series : Topics in Epilepsy
Find out the books of Topics in Epilepsy
ISBN : 978-2-7420-0810-0
112 pages
Specialty : Neurology, Epilepsy, Neurology, Epilepsy
Published in : English
Format : 17x24 cm
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37.00 € |
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More than half of epilepsies start before the age of 20 years and nearly 25% of them are refractory.
A tiny proportion of them are even labelled a “rare illness”, i.e. one affecting less than 200,000 people in the United States or less than 5 out of 10,000 people in the European Union.
For these patients, two problems in their management arise:
- In children, seizures affect an immature brain and can impact its development. It is therefore essential to treat them so that brain development continues as normally as possible.
- The rarity of these syndromes does not encourage the pharmaceutical industry to invest in research.
Therefore, there are few drugs available.
However, a few target syndromes with a particularly unfavourable diagnosis. This work outlines 6 molecules in detail that are specifically used in epileptic encephalopathies. Every aspect of these molecules is discussed, including drug development, indication, efficacy, cost, etc.
Drafted by international experts in the field of epileptology, it provides all the necessary information on orphan drugs and their clinical use.
SUMMARY
Bromides
Corticosteroids and adrenocorticotropic hormone
Vigabatrin
Stiripentol
Felbamate
Rufinamide
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