Noonan syndrome (NS) is an autosomal dominant disorder commonly caused by PTPN11 germline mutations. Patients are characterized by short stature, congenital heart defects, facial dysmorphism, and increased risk of malignancies including brain tumors. Commonly associated brain tumors are dysembryoplastic neuroepithelial tumor and low-grade glioma. We report two cases of anaplastic astrocytoma with PTPN11-related NS. We conducted a systematic search of medical databases looking for other reported cases of high-grade glioma associated with NS and identified 24 cases of brain tumors, all of which were low-grade glial or glioneuronal tumors except for one case of medulloblastoma
peer reviewedMutations in LZTR1, already known to be causal in familial schwannomatosis type 2, have...
Noonan syndrome (NS) is an autosomal dominant disorder characterized by short stature, typical crani...
Noonan syndrome (NS) is an autosomal dominant disorder caused by mutations in PTPN11, KRAS, SOS1, an...
Noonan syndrome (NS) is a congenital autosomic dominant condition characterized by a variable spectr...
Noonan syndrome (NS) is a congenital autosomic dominant condition characterized by a variable spectr...
Noonan syndrome (NS) is an autosomal dominant developmental disorder caused by mutations in the RAS-...
Noonan syndrome (NS) is an autosomal dominant disease caused by aberrant up-regulated signaling thro...
6sinonemixedPellegrin MC, Tornese G, Cattaruzzi E, Blank E, Kieslich M, Ventura A.Pellegrin, Mc; Tor...
Mutations in LZTR1, already known to be causal in familial schwannomatosis type 2, have been recentl...
Noonan syndrome (NS) is an autosomal dominant disorder, characterized by short stature, minor facial...
Noonan syndrome (NS) is an autosomal dominant disorder, characterized by short stature, minor facial...
Noonan syndrome (NS) is an autosomal dominant disorder caused by mutations in PTPN11, KRAS, SOS1, an...
Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genet...
Noonan syndrome (NS) is an autosomal dominant disorder, characterized by short stature, minor facial...
Item does not contain fulltextNoonan syndrome is a well-known clinical entity comprising multiple co...
peer reviewedMutations in LZTR1, already known to be causal in familial schwannomatosis type 2, have...
Noonan syndrome (NS) is an autosomal dominant disorder characterized by short stature, typical crani...
Noonan syndrome (NS) is an autosomal dominant disorder caused by mutations in PTPN11, KRAS, SOS1, an...
Noonan syndrome (NS) is a congenital autosomic dominant condition characterized by a variable spectr...
Noonan syndrome (NS) is a congenital autosomic dominant condition characterized by a variable spectr...
Noonan syndrome (NS) is an autosomal dominant developmental disorder caused by mutations in the RAS-...
Noonan syndrome (NS) is an autosomal dominant disease caused by aberrant up-regulated signaling thro...
6sinonemixedPellegrin MC, Tornese G, Cattaruzzi E, Blank E, Kieslich M, Ventura A.Pellegrin, Mc; Tor...
Mutations in LZTR1, already known to be causal in familial schwannomatosis type 2, have been recentl...
Noonan syndrome (NS) is an autosomal dominant disorder, characterized by short stature, minor facial...
Noonan syndrome (NS) is an autosomal dominant disorder, characterized by short stature, minor facial...
Noonan syndrome (NS) is an autosomal dominant disorder caused by mutations in PTPN11, KRAS, SOS1, an...
Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genet...
Noonan syndrome (NS) is an autosomal dominant disorder, characterized by short stature, minor facial...
Item does not contain fulltextNoonan syndrome is a well-known clinical entity comprising multiple co...
peer reviewedMutations in LZTR1, already known to be causal in familial schwannomatosis type 2, have...
Noonan syndrome (NS) is an autosomal dominant disorder characterized by short stature, typical crani...
Noonan syndrome (NS) is an autosomal dominant disorder caused by mutations in PTPN11, KRAS, SOS1, an...