Bartelt-Kirbach B, Wuepping M, Dodrimont-Lattke M, Kaufmann D
Institute of Human Genetics, University of Ulm, Ulm, Germany.
Neurogenetics. 2009 Feb;10(1):79-85. doi: 10.1007/s10048-008-0154-0. Epub 2008 Oct 11.
The hallmark of neurofibromatosis type 1 (NF1) are multiple dermal neurofibromas. They show high inter- and intrafamilial variability for which the influence of modifying genes is discussed. NF1 patients presenting microdeletions spanning NF1 and several contiguous genes have an earlier onset and higher number of dermal neurofibromas than classical NF1 patients, pointing to one of the deleted genes as modifier. Expression analysis of 13 genes of the microdeletion region in dermal neurofibromas and other tissues revealed four candidates for the modification of neurofibroma formation: CENTA2, RAB11FIP4, C17orf79, and UTP6.
1型神经纤维瘤病(NF1)的标志是多发性皮肤神经纤维瘤。它们在家族间和家族内表现出高度变异性,对此人们讨论了修饰基因的影响。与典型NF1患者相比,呈现跨越NF1和几个相邻基因的微缺失的NF1患者发病更早,皮肤神经纤维瘤数量更多,这表明其中一个缺失基因是修饰基因。对皮肤神经纤维瘤和其他组织中微缺失区域的13个基因进行表达分析,发现了4个影响神经纤维瘤形成的候选基因:CENTA2、RAB11FIP4、C17orf79和UTP6。