Barnabás Péter Botos, Júlia Erhardt, Sámuel Jenei, Kamilla Luca Li, Dávid Sándor Kovács, Bálint Egyed, Jusztina Nikolett Beniczky, Dániel Erdélyi, Judit Müller, Edit Brückner, Monika Csóka, Andrea Szabó, László Környei, Rita Bertalan, Gábor Kovács, Csaba Vilmányi, Miklós Garami, Csaba Bödör, Ferenc Árpád Kovács
{"title":"[RAS病的诊断和治疗前景]。","authors":"Barnabás Péter Botos, Júlia Erhardt, Sámuel Jenei, Kamilla Luca Li, Dávid Sándor Kovács, Bálint Egyed, Jusztina Nikolett Beniczky, Dániel Erdélyi, Judit Müller, Edit Brückner, Monika Csóka, Andrea Szabó, László Környei, Rita Bertalan, Gábor Kovács, Csaba Vilmányi, Miklós Garami, Csaba Bödör, Ferenc Árpád Kovács","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>RASopathies are congenital diseases that manifest in childhood with symptoms and potential complications, typically associated with an elevated tumour predisposition risk. The heterogeneous symptoms involve mostly central nervous, cardiovascular, musculoskeletal systems and skin, and modified growth pattern. From molecular perspective, the function of a key protein involved in Ras signalling is impaired, leading to disrupted regulation of cell growth and division. It is crucial to uncover genetic history, analyse tumour and cardiac involvement pattern along four generation pedigree and depict minor anomaly pattern. Upon clinical suspicion a stepwise approach to molecular testing is recommended to confirm or rule out the specific RASopathy. Post-test genetic counselling should address potential complications, developmental and follow-up strategies in line with current guidelines. Cascade pedigree segregation analysis according to the inheritance pattern should be offered to family planning parents and potentially affected family members. In case of certain specific organ involvement or complications, targeted therapeutics are available, highlighting the importance of early diagnosis.</p>","PeriodicalId":94127,"journal":{"name":"Magyar onkologia","volume":"68 4","pages":"313"},"PeriodicalIF":0.0000,"publicationDate":"2024-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Diagnostic and therapeutic perspectives in RASopathies].\",\"authors\":\"Barnabás Péter Botos, Júlia Erhardt, Sámuel Jenei, Kamilla Luca Li, Dávid Sándor Kovács, Bálint Egyed, Jusztina Nikolett Beniczky, Dániel Erdélyi, Judit Müller, Edit Brückner, Monika Csóka, Andrea Szabó, László Környei, Rita Bertalan, Gábor Kovács, Csaba Vilmányi, Miklós Garami, Csaba Bödör, Ferenc Árpád Kovács\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>RASopathies are congenital diseases that manifest in childhood with symptoms and potential complications, typically associated with an elevated tumour predisposition risk. The heterogeneous symptoms involve mostly central nervous, cardiovascular, musculoskeletal systems and skin, and modified growth pattern. From molecular perspective, the function of a key protein involved in Ras signalling is impaired, leading to disrupted regulation of cell growth and division. It is crucial to uncover genetic history, analyse tumour and cardiac involvement pattern along four generation pedigree and depict minor anomaly pattern. Upon clinical suspicion a stepwise approach to molecular testing is recommended to confirm or rule out the specific RASopathy. Post-test genetic counselling should address potential complications, developmental and follow-up strategies in line with current guidelines. Cascade pedigree segregation analysis according to the inheritance pattern should be offered to family planning parents and potentially affected family members. In case of certain specific organ involvement or complications, targeted therapeutics are available, highlighting the importance of early diagnosis.</p>\",\"PeriodicalId\":94127,\"journal\":{\"name\":\"Magyar onkologia\",\"volume\":\"68 4\",\"pages\":\"313\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-12-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Magyar onkologia\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/11/19 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Magyar onkologia","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/19 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
[Diagnostic and therapeutic perspectives in RASopathies].
RASopathies are congenital diseases that manifest in childhood with symptoms and potential complications, typically associated with an elevated tumour predisposition risk. The heterogeneous symptoms involve mostly central nervous, cardiovascular, musculoskeletal systems and skin, and modified growth pattern. From molecular perspective, the function of a key protein involved in Ras signalling is impaired, leading to disrupted regulation of cell growth and division. It is crucial to uncover genetic history, analyse tumour and cardiac involvement pattern along four generation pedigree and depict minor anomaly pattern. Upon clinical suspicion a stepwise approach to molecular testing is recommended to confirm or rule out the specific RASopathy. Post-test genetic counselling should address potential complications, developmental and follow-up strategies in line with current guidelines. Cascade pedigree segregation analysis according to the inheritance pattern should be offered to family planning parents and potentially affected family members. In case of certain specific organ involvement or complications, targeted therapeutics are available, highlighting the importance of early diagnosis.