Pathogenesis of vestibular schwannoma in ring chromosome 22
<p>Abstract</p> <p>Background</p> <p>Ring chromosome 22 is a rare human constitutional cytogenetic abnormality. Clinical features of neurofibromatosis type 1 and 2 as well as different tumour types have been reported in patients with ring chromosome 22. The pathogenesis...
Main Authors: | Debiec-Rychter Maria, Sciot Raf, Bowers Naomi, Van Calenbergh Frank, Evans Gareth D, de Cock Paul, Brems Hilde, Denayer Ellen, Vermeesch Joris V, Fryns Jean-Pierre, Legius Eric |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2009-09-01
|
Series: | BMC Medical Genetics |
Online Access: | http://www.biomedcentral.com/1471-2350/10/97 |
Similar Items
-
A rare case of atypical/anaplastic meningioma with MDM2 amplification
by: Robbert Wylleman, et al.
Published: (2018-05-01) -
Legius Syndrome and its Relationship with Neurofibromatosis Type 1
by: Ellen Denayer, et al.
Published: (2020-03-01) -
Radiosurgery for vestibular schwannomas
by: Sumit Sinha, et al.
Published: (2014-09-01) -
Surgery of vestibular schwannomas
by: Madjid Samii, et al.
Published: (2012-01-01) -
Intraosseous schwannoma of the glenoid: case report and literature review
by: Reyniers Pieter, et al.
Published: (2021-01-01)