Article
Rosette forming glioneuronal tumor in association with Noonan syndrome: pathobiological implications.
Clinical neuropathology - 1 Jan 2000
Karafin M, Jallo G I, Ayars M, Eberhart C G, Rodriguez F J
Abstract excerpt
Noonan syndrome, a distinctive syndrome characterized by dysmorphism, cardiac abnormalities and developmental delay, has been associated with a number of malignancies, however, only a few cases of primary glial or glioneuronal neoplasms have been reported. We report here the case of an 18-year-old with Noonan syndrome who developed a rosette forming glioneuronal tumor of the posterior fossa. The tumor...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.