Wir verwenden Cookies und Analyse-Tools, um die Nutzerfreundlichkeit der Internet-Seite zu verbessern und für Marketingzwecke. Wenn Sie fortfahren, diese Seite zu verwenden, nehmen wir an, dass Sie damit einverstanden sind. Zur Datenschutzerklärung.
Neurofibromatosis Type II
CHF 43.15
Auf Lager
SKU
TOB49JJDD1T
1 Verfügbar 
Geliefert zwischen Fr., 14.11.2025 und Mo., 17.11.2025
Details
Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Neurofibromatosis Type II (or "MISME Syndrome", for "Multiple Inherited Schwannomas, Meningiomas, and Ependymomas") is an inherited disease. The main manifestation of the disease is the development of symmetric, non-malignant brain tumours in the region of the cranial nerve VIII, which is the auditory-vestibular nerve that transmits sensory information from the inner ear to the brain. Most people with this condition also experience problems in their eyes. NF II is caused by mutations of the "Merlin" gene, which, it seems, influences the form and movement of cells. The principal treatments consist of neurosurgical removal of the tumors and surgical treatment of the eye lesions. There is no therapy for the underlying disorder of cell function caused by the genetic mutation.
Weitere Informationen
- Allgemeine Informationen
- Editor Lambert M. Surhone, Mariam T. Tennoe, Susan F. Henssonow
- Titel Neurofibromatosis Type II
- Format Fachbuch
- EAN 9786131271373
- Größe H5mm x B220mm x T150mm
- Gewicht 144g
- Genre Medizin
- Anzahl Seiten 96
- Herausgeber Betascript Publishing
- GTIN 09786131271373
Bewertungen
Schreiben Sie eine Bewertung
