Lubs H A, Chiurazzi P, Arena J F, Schwartz C, Tranebjaerg L, Neri G
Department of Medical Genetics, University Hospital of Tromsø, Norway.
Am J Med Genet. 1996 Jul 12;64(1):147-57. doi: 10.1002/(SICI)1096-8628(19960712)64:1<147::AID-AJMG25>3.0.CO;2-M.
A current list of all known forms of X-linked mental retardation (XLMR) and a slightly revised classification are presented. The number of known disorders has not increased because 6 disorders have been combined based on new molecular data or on clinical grounds and only 6 newly described XLMR disorders have been reported. Of the current 105 XLMR disorders, 34 have been mapped, and 18 disorders and 1 nonspecific XLMR (FRAXE) have been cloned. The number of families with nonspecific XLMR with a LOD score of > or = 2.0 has more than doubled, with 42 (including FRAXE) now being known. a summary of the localization of presumed nonspecific mental retardation (MR) genes from well-studied X-chromosomal translocations and deletions is also included. Only 10-12 nonoverlapping loci are required to explain all localizations of nonspecific MR from both approaches. These new trends mark the beginning of a significantly improved understanding of the role of genes on the X chromosome in producing MR. Continued close collaboration between clinical and molecular investigators will be required to complete the process.
本文列出了所有已知的X连锁智力迟钝(XLMR)形式的最新列表以及一个略有修订的分类。已知疾病的数量没有增加,因为基于新的分子数据或临床依据,有6种疾病被合并,并且仅报告了6种新描述的XLMR疾病。在目前已知的105种XLMR疾病中,34种已被定位,18种疾病和1种非特异性XLMR(FRAXE)已被克隆。LOD评分≥2.0的非特异性XLMR家族数量增加了一倍多,目前已知有42个(包括FRAXE)。本文还总结了来自经过充分研究的X染色体易位和缺失的假定非特异性智力迟钝(MR)基因的定位情况。两种方法只需10 - 12个不重叠的基因座就能解释所有非特异性MR的定位。这些新趋势标志着对X染色体上基因在导致MR中所起作用的理解有了显著改善的开端。临床和分子研究人员之间需要持续密切合作以完成这一进程。