父母患有节段性神经纤维瘤病的孩子的1型神经纤维瘤病(NF-5)。

Neurofibromatosis Pub Date : 1989-01-01

E Boltshauser, H Stocker, M Mächler

{"title":"父母患有节段性神经纤维瘤病的孩子的1型神经纤维瘤病(NF-5)。","authors":"E Boltshauser, H Stocker, M Mächler","doi":"","DOIUrl":null,"url":null,"abstract":"Neurofibromatosis type 1 (NF-1) was incidentally diagnosed in a 1-year-old girl. Her father was found to show the cutaneous signs of segmental neurofibromatosis (NF-5). This observation supports the possibility that subjects with NF-5 can transmit NF-1 to their offsprings in some cases, which has to be considered in genetic counseling.","PeriodicalId":77754,"journal":{"name":"Neurofibromatosis","volume":"2 4","pages":"244-5"},"PeriodicalIF":0.0000,"publicationDate":"1989-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Neurofibromatosis type 1 in a child of a parent with segmental neurofibromatosis (NF-5).\",\"authors\":\"E Boltshauser, H Stocker, M Mächler\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Neurofibromatosis type 1 (NF-1) was incidentally diagnosed in a 1-year-old girl. Her father was found to show the cutaneous signs of segmental neurofibromatosis (NF-5). This observation supports the possibility that subjects with NF-5 can transmit NF-1 to their offsprings in some cases, which has to be considered in genetic counseling.\",\"PeriodicalId\":77754,\"journal\":{\"name\":\"Neurofibromatosis\",\"volume\":\"2 4\",\"pages\":\"244-5\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1989-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Neurofibromatosis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurofibromatosis","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}

引用次数: 0

摘要

1型神经纤维瘤病(NF-1)被偶然诊断为1岁女孩。她的父亲被发现有节段性神经纤维瘤病(NF-5)的皮肤征象。这一观察结果支持了NF-5受试者在某些情况下将NF-1遗传给后代的可能性，这在遗传咨询中必须考虑到。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

本刊更多论文

Neurofibromatosis type 1 in a child of a parent with segmental neurofibromatosis (NF-5).

Neurofibromatosis type 1 (NF-1) was incidentally diagnosed in a 1-year-old girl. Her father was found to show the cutaneous signs of segmental neurofibromatosis (NF-5). This observation supports the possibility that subjects with NF-5 can transmit NF-1 to their offsprings in some cases, which has to be considered in genetic counseling.

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

Neurofibromatosis

自引率

0.00%

发文量