D Bettio, D Giardino, N Rizzi, P Riva, L Volpi, E Barantani, A Tagliaferri, L Larizza
{"title":"垂体腺瘤Prader-Willi患者母体来源的同染色体15q。","authors":"D Bettio, D Giardino, N Rizzi, P Riva, L Volpi, E Barantani, A Tagliaferri, L Larizza","doi":"10.1017/s000156600000132x","DOIUrl":null,"url":null,"abstract":"<p><p>We report on a Prader-Willi syndrome (PWS) patient carrier of a balanced 15q15q translocation and affected by a prolactin-secreting pituitary adenoma. Evidence provided by molecular studies indicates that the structural rearrangement is an isochromosome of maternal origin. According to the identification of isodisomy as the basis of the association of rare disorders and the recent report on chromosome 15 monosomy and nullisomy in pituitary adenoma, we suggest that in our case PWS and pituitary adenoma might be related.</p>","PeriodicalId":7118,"journal":{"name":"Acta geneticae medicae et gemellologiae","volume":"45 1-2","pages":"213-6"},"PeriodicalIF":0.0000,"publicationDate":"1996-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1017/s000156600000132x","citationCount":"9","resultStr":"{\"title\":\"Isochromosome 15q of maternal origin in a Prader-Willi patient with pituitary adenoma.\",\"authors\":\"D Bettio, D Giardino, N Rizzi, P Riva, L Volpi, E Barantani, A Tagliaferri, L Larizza\",\"doi\":\"10.1017/s000156600000132x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>We report on a Prader-Willi syndrome (PWS) patient carrier of a balanced 15q15q translocation and affected by a prolactin-secreting pituitary adenoma. Evidence provided by molecular studies indicates that the structural rearrangement is an isochromosome of maternal origin. According to the identification of isodisomy as the basis of the association of rare disorders and the recent report on chromosome 15 monosomy and nullisomy in pituitary adenoma, we suggest that in our case PWS and pituitary adenoma might be related.</p>\",\"PeriodicalId\":7118,\"journal\":{\"name\":\"Acta geneticae medicae et gemellologiae\",\"volume\":\"45 1-2\",\"pages\":\"213-6\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1996-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1017/s000156600000132x\",\"citationCount\":\"9\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta geneticae medicae et gemellologiae\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1017/s000156600000132x\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta geneticae medicae et gemellologiae","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1017/s000156600000132x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Isochromosome 15q of maternal origin in a Prader-Willi patient with pituitary adenoma.
We report on a Prader-Willi syndrome (PWS) patient carrier of a balanced 15q15q translocation and affected by a prolactin-secreting pituitary adenoma. Evidence provided by molecular studies indicates that the structural rearrangement is an isochromosome of maternal origin. According to the identification of isodisomy as the basis of the association of rare disorders and the recent report on chromosome 15 monosomy and nullisomy in pituitary adenoma, we suggest that in our case PWS and pituitary adenoma might be related.