Familial melanoma-astrocytoma syndrome: synchronous diffuse astrocytoma and pleomorphic xanthoastrocytoma in a patient with germline CDKN2A/B deletion and a significant family history

Familial melanoma-astrocytoma syndrome is a tumor predisposition syndrome caused by inactivating germline alteration of the CDKN2A tumor suppressor gene on chromosome 9p21. While some families with germline CDKN2A mutations are prone to development of just melanomas, other families develop both mela...

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Detalles Bibliográficos
Autores principales: Chan, Andrew K., Han, Seunggu J., Choy, Winward, Beleford, Daniah, Aghi, Manish K., Berger, Mitchel S., Shieh, Joseph T., Bollen, Andrew W., Perry, Arie, Phillips, Joanna J., Butowski, Nicholas, Solomon, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dustri-Verlag Dr. Karl Feistle 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5628627/
https://www.ncbi.nlm.nih.gov/pubmed/28699883
http://dx.doi.org/10.5414/NP301022

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5628627/
https://www.ncbi.nlm.nih.gov/pubmed/28699883
http://dx.doi.org/10.5414/NP301022

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