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NSRG-07. TURCOT SYNDROME: A SYNCHRONOUS CLINICAL PRESENTATION OF MEDULLOBLASTOMA AND LOWER RECTAL TUMOR

INTRODUCTION: Turcot syndrome (TS) is a rare hereditary disorder with genetic susceptibility to cancer which is characterized by the occurrence of colorectal and central nervous system (CNS) tumors. CLINICAL CASE: Here we report the case of a 16-year-old patient who was operated for medulloblastoma...

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Dades bibliogràfiques
Publicat a:Neuro Oncol
Autors principals: Borni, Mehdi, Kolsi, Fatma, Abdelhedi, Anis, Jarraya, Firas, Boudawara, Mohammed Zaher
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2018
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6011972/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/noy059.529
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