Occurrence of high-grade glioma in Noonan syndrome : report of two cases
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 dysembryopla...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
El-Ayadi, Moatasem [verfasserIn] Ansari, Marc [verfasserIn] Kühnöl, Caspar David - 1978- [verfasserIn] Bendel, Anne [verfasserIn] Sturm, Dominik - 1983- [verfasserIn] Pietsch, Torsten [verfasserIn] Kramm, Christof M. [verfasserIn] Büren, André O. von [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
28 January 2019 |
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| Schlagwörter: |
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| Anmerkung: |
Gesehen am 04.04.2019 |
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| Umfang: |
4 |
| Übergeordnetes Werk: |
Enthalten in: Pediatric blood & cancer - New York, NY : Wiley, 2004, 66(2019,5) Artikelnummer e27625, 4 Seiten |
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| Übergeordnetes Werk: |
volume:66 ; year:2019 ; number:5 ; pages:e27625 ; extent:4 |
| Links: |
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| DOI / URN: |
10.1002/pbc.27625 |
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| Katalog-ID: |
1662830696 |
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| 245 | 1 | 0 | |a Occurrence of high-grade glioma in Noonan syndrome |b report of two cases |c Moatasem El‐Ayadi, Marc Ansari, Caspar D. Kühnöl, Anne Bendel, Dominik Sturm, Torsten Pietsch, Christof M. Kramm, André O. von Bueren |
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| 520 | |a 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. | ||
| 650 | 4 | |a brain tumor | |
| 650 | 4 | |a high-grade glioma | |
| 650 | 4 | |a Noonan syndrome | |
| 650 | 4 | |a PTPN11 mutations | |
| 650 | 4 | |a RASopathy | |
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| 700 | 1 | |a Bendel, Anne |e verfasserin |4 aut | |
| 700 | 1 | |a Sturm, Dominik |d 1983- |e verfasserin |0 (DE-588)1035550709 |0 (DE-627)749549165 |0 (DE-576)383282144 |4 aut | |
| 700 | 1 | |a Pietsch, Torsten |e verfasserin |4 aut | |
| 700 | 1 | |a Kramm, Christof M. |e verfasserin |4 aut | |
| 700 | 1 | |a Büren, André O. von |e verfasserin |4 aut | |
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10.1002/pbc.27625 doi (DE-627)1662830696 (DE-599)KXP1662830696 (OCoLC)1341207925 DE-627 ger DE-627 rda eng El-Ayadi, Moatasem verfasserin (DE-588)1172430926 (DE-627)1041200072 (DE-576)514617136 aut Occurrence of high-grade glioma in Noonan syndrome report of two cases Moatasem El‐Ayadi, Marc Ansari, Caspar D. Kühnöl, Anne Bendel, Dominik Sturm, Torsten Pietsch, Christof M. Kramm, André O. von Bueren 28 January 2019 4 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Gesehen am 04.04.2019 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. brain tumor high-grade glioma Noonan syndrome PTPN11 mutations RASopathy Ansari, Marc verfasserin aut Kühnöl, Caspar David 1978- verfasserin (DE-588)143829173 (DE-627)704614111 (DE-576)339185945 aut Bendel, Anne verfasserin aut Sturm, Dominik 1983- verfasserin (DE-588)1035550709 (DE-627)749549165 (DE-576)383282144 aut Pietsch, Torsten verfasserin aut Kramm, Christof M. verfasserin aut Büren, André O. von verfasserin aut Enthalten in Pediatric blood & cancer New York, NY : Wiley, 2004 66(2019,5) Artikelnummer e27625, 4 Seiten Online-Ressource (DE-627)37682798X (DE-600)2130978-4 (DE-576)11281610X 1545-5017 nnns volume:66 year:2019 number:5 pages:e27625 extent:4 https://doi.org/10.1002/pbc.27625 Verlag Resolving-System Volltext https://onlinelibrary.wiley.com/doi/abs/10.1002/pbc.27625 Verlag Volltext GBV_USEFLAG_U GBV_ILN_64 SYSFLAG_1 GBV_KXP GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 GBV_ILN_2013 GBV_ILN_2013 ISIL_DE-16-250 AR 66 2019 5 e27625 4 66(2019,5) Artikelnummer e27625, 4 Seiten 64 01 3064 3686682923 x 12-06-20 2013 01 DE-16-250 3418120857 00 --%%-- --%%-- --%%-- --%%-- l01 04-04-19 64 00 3064 00 (DE-627)1041828608 Universitätsklinik und Poliklinik für Pädiatrie I <Halle, Saale> 64 00 3064 01 (DE-627)355383683 Zeitschrift 64 00 3064 02 (DE-627)355383330 Aufsatz 2013 01 DE-16-250 00 s hd2019 2013 01 DE-16-250 01 s (DE-627)1410508463 wissenschaftlicher Artikel (Zeitschrift) 2013 01 DE-16-250 02 s per_8 2013 01 DE-16-250 03 s s_4 2013 01 DE-16-250 04 p (DE-627)1465968652 Sturm, Dominik 2013 01 DE-16-250 04 k (DE-627)1416740988 Zentrum für Kinder- und Jugendmedizin 2013 01 DE-16-250 04 s (DE-627)1410501914 Verfasser 2013 01 DE-16-250 04 s pos_5 64 01 3064 99 j2019 |
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10.1002/pbc.27625 doi (DE-627)1662830696 (DE-599)KXP1662830696 (OCoLC)1341207925 DE-627 ger DE-627 rda eng El-Ayadi, Moatasem verfasserin (DE-588)1172430926 (DE-627)1041200072 (DE-576)514617136 aut Occurrence of high-grade glioma in Noonan syndrome report of two cases Moatasem El‐Ayadi, Marc Ansari, Caspar D. Kühnöl, Anne Bendel, Dominik Sturm, Torsten Pietsch, Christof M. Kramm, André O. von Bueren 28 January 2019 4 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Gesehen am 04.04.2019 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. brain tumor high-grade glioma Noonan syndrome PTPN11 mutations RASopathy Ansari, Marc verfasserin aut Kühnöl, Caspar David 1978- verfasserin (DE-588)143829173 (DE-627)704614111 (DE-576)339185945 aut Bendel, Anne verfasserin aut Sturm, Dominik 1983- verfasserin (DE-588)1035550709 (DE-627)749549165 (DE-576)383282144 aut Pietsch, Torsten verfasserin aut Kramm, Christof M. verfasserin aut Büren, André O. von verfasserin aut Enthalten in Pediatric blood & cancer New York, NY : Wiley, 2004 66(2019,5) Artikelnummer e27625, 4 Seiten Online-Ressource (DE-627)37682798X (DE-600)2130978-4 (DE-576)11281610X 1545-5017 nnns volume:66 year:2019 number:5 pages:e27625 extent:4 https://doi.org/10.1002/pbc.27625 Verlag Resolving-System Volltext https://onlinelibrary.wiley.com/doi/abs/10.1002/pbc.27625 Verlag Volltext GBV_USEFLAG_U GBV_ILN_64 SYSFLAG_1 GBV_KXP GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 GBV_ILN_2013 GBV_ILN_2013 ISIL_DE-16-250 AR 66 2019 5 e27625 4 66(2019,5) Artikelnummer e27625, 4 Seiten 64 01 3064 3686682923 x 12-06-20 2013 01 DE-16-250 3418120857 00 --%%-- --%%-- --%%-- --%%-- l01 04-04-19 64 00 3064 00 (DE-627)1041828608 Universitätsklinik und Poliklinik für Pädiatrie I <Halle, Saale> 64 00 3064 01 (DE-627)355383683 Zeitschrift 64 00 3064 02 (DE-627)355383330 Aufsatz 2013 01 DE-16-250 00 s hd2019 2013 01 DE-16-250 01 s (DE-627)1410508463 wissenschaftlicher Artikel (Zeitschrift) 2013 01 DE-16-250 02 s per_8 2013 01 DE-16-250 03 s s_4 2013 01 DE-16-250 04 p (DE-627)1465968652 Sturm, Dominik 2013 01 DE-16-250 04 k (DE-627)1416740988 Zentrum für Kinder- und Jugendmedizin 2013 01 DE-16-250 04 s (DE-627)1410501914 Verfasser 2013 01 DE-16-250 04 s pos_5 64 01 3064 99 j2019 |
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10.1002/pbc.27625 doi (DE-627)1662830696 (DE-599)KXP1662830696 (OCoLC)1341207925 DE-627 ger DE-627 rda eng El-Ayadi, Moatasem verfasserin (DE-588)1172430926 (DE-627)1041200072 (DE-576)514617136 aut Occurrence of high-grade glioma in Noonan syndrome report of two cases Moatasem El‐Ayadi, Marc Ansari, Caspar D. Kühnöl, Anne Bendel, Dominik Sturm, Torsten Pietsch, Christof M. Kramm, André O. von Bueren 28 January 2019 4 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Gesehen am 04.04.2019 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. brain tumor high-grade glioma Noonan syndrome PTPN11 mutations RASopathy Ansari, Marc verfasserin aut Kühnöl, Caspar David 1978- verfasserin (DE-588)143829173 (DE-627)704614111 (DE-576)339185945 aut Bendel, Anne verfasserin aut Sturm, Dominik 1983- verfasserin (DE-588)1035550709 (DE-627)749549165 (DE-576)383282144 aut Pietsch, Torsten verfasserin aut Kramm, Christof M. verfasserin aut Büren, André O. von verfasserin aut Enthalten in Pediatric blood & cancer New York, NY : Wiley, 2004 66(2019,5) Artikelnummer e27625, 4 Seiten Online-Ressource (DE-627)37682798X (DE-600)2130978-4 (DE-576)11281610X 1545-5017 nnns volume:66 year:2019 number:5 pages:e27625 extent:4 https://doi.org/10.1002/pbc.27625 Verlag Resolving-System Volltext https://onlinelibrary.wiley.com/doi/abs/10.1002/pbc.27625 Verlag Volltext GBV_USEFLAG_U GBV_ILN_64 SYSFLAG_1 GBV_KXP GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 GBV_ILN_2013 GBV_ILN_2013 ISIL_DE-16-250 AR 66 2019 5 e27625 4 66(2019,5) Artikelnummer e27625, 4 Seiten 64 01 3064 3686682923 x 12-06-20 2013 01 DE-16-250 3418120857 00 --%%-- --%%-- --%%-- --%%-- l01 04-04-19 64 00 3064 00 (DE-627)1041828608 Universitätsklinik und Poliklinik für Pädiatrie I <Halle, Saale> 64 00 3064 01 (DE-627)355383683 Zeitschrift 64 00 3064 02 (DE-627)355383330 Aufsatz 2013 01 DE-16-250 00 s hd2019 2013 01 DE-16-250 01 s (DE-627)1410508463 wissenschaftlicher Artikel (Zeitschrift) 2013 01 DE-16-250 02 s per_8 2013 01 DE-16-250 03 s s_4 2013 01 DE-16-250 04 p (DE-627)1465968652 Sturm, Dominik 2013 01 DE-16-250 04 k (DE-627)1416740988 Zentrum für Kinder- und Jugendmedizin 2013 01 DE-16-250 04 s (DE-627)1410501914 Verfasser 2013 01 DE-16-250 04 s pos_5 64 01 3064 99 j2019 |
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10.1002/pbc.27625 doi (DE-627)1662830696 (DE-599)KXP1662830696 (OCoLC)1341207925 DE-627 ger DE-627 rda eng El-Ayadi, Moatasem verfasserin (DE-588)1172430926 (DE-627)1041200072 (DE-576)514617136 aut Occurrence of high-grade glioma in Noonan syndrome report of two cases Moatasem El‐Ayadi, Marc Ansari, Caspar D. Kühnöl, Anne Bendel, Dominik Sturm, Torsten Pietsch, Christof M. Kramm, André O. von Bueren 28 January 2019 4 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Gesehen am 04.04.2019 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. brain tumor high-grade glioma Noonan syndrome PTPN11 mutations RASopathy Ansari, Marc verfasserin aut Kühnöl, Caspar David 1978- verfasserin (DE-588)143829173 (DE-627)704614111 (DE-576)339185945 aut Bendel, Anne verfasserin aut Sturm, Dominik 1983- verfasserin (DE-588)1035550709 (DE-627)749549165 (DE-576)383282144 aut Pietsch, Torsten verfasserin aut Kramm, Christof M. verfasserin aut Büren, André O. von verfasserin aut Enthalten in Pediatric blood & cancer New York, NY : Wiley, 2004 66(2019,5) Artikelnummer e27625, 4 Seiten Online-Ressource (DE-627)37682798X (DE-600)2130978-4 (DE-576)11281610X 1545-5017 nnns volume:66 year:2019 number:5 pages:e27625 extent:4 https://doi.org/10.1002/pbc.27625 Verlag Resolving-System Volltext https://onlinelibrary.wiley.com/doi/abs/10.1002/pbc.27625 Verlag Volltext GBV_USEFLAG_U GBV_ILN_64 SYSFLAG_1 GBV_KXP GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 GBV_ILN_2013 GBV_ILN_2013 ISIL_DE-16-250 AR 66 2019 5 e27625 4 66(2019,5) Artikelnummer e27625, 4 Seiten 64 01 3064 3686682923 x 12-06-20 2013 01 DE-16-250 3418120857 00 --%%-- --%%-- --%%-- --%%-- l01 04-04-19 64 00 3064 00 (DE-627)1041828608 Universitätsklinik und Poliklinik für Pädiatrie I <Halle, Saale> 64 00 3064 01 (DE-627)355383683 Zeitschrift 64 00 3064 02 (DE-627)355383330 Aufsatz 2013 01 DE-16-250 00 s hd2019 2013 01 DE-16-250 01 s (DE-627)1410508463 wissenschaftlicher Artikel (Zeitschrift) 2013 01 DE-16-250 02 s per_8 2013 01 DE-16-250 03 s s_4 2013 01 DE-16-250 04 p (DE-627)1465968652 Sturm, Dominik 2013 01 DE-16-250 04 k (DE-627)1416740988 Zentrum für Kinder- und Jugendmedizin 2013 01 DE-16-250 04 s (DE-627)1410501914 Verfasser 2013 01 DE-16-250 04 s pos_5 64 01 3064 99 j2019 |
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Occurrence of high-grade glioma in Noonan syndrome report of two cases |
| abstract |
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. Gesehen am 04.04.2019 |
| abstractGer |
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. Gesehen am 04.04.2019 |
| abstract_unstemmed |
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. Gesehen am 04.04.2019 |
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| container_issue |
5 |
| title_short |
Occurrence of high-grade glioma in Noonan syndrome |
| url |
https://doi.org/10.1002/pbc.27625 https://onlinelibrary.wiley.com/doi/abs/10.1002/pbc.27625 |
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Ansari, Marc Kühnöl, Caspar David 1978- Bendel, Anne Sturm, Dominik 1983- Pietsch, Torsten Kramm, Christof M. Büren, André O. von |
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Ansari, Marc Kühnöl, Caspar David 1978- Bendel, Anne Sturm, Dominik 1983- Pietsch, Torsten Kramm, Christof M. Büren, André O. von |
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Ayadi, Moatasem el- El-Ayadi, Moatasem Kühnöl, Caspar David Sturm, Markus Dominik Sturm, Dominik |
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10.1002/pbc.27625 |
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| up_date |
2024-07-04T12:09:59.575Z |
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