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X连锁智力迟钝(XLMR)研究:迈阿密/格林伍德研究中61个家庭的总结

Study of X-linked mental retardation (XLMR): summary of 61 families in the Miami/Greenwood Study.

作者信息

Lubs H A, Schwartz C E, Stevenson R E, Arena J F

机构信息

Department of Pediatrics, University of Miami, Florida, USA.

出版信息

Am J Med Genet. 1996 Jul 12;64(1):169-75. doi: 10.1002/(SICI)1096-8628(19960712)64:1<169::AID-AJMG29>3.0.CO;2-K.

Abstract

The initial goal of this study was to localize as many genes as possible that lead to syndromic and nonspecific XLMR. More recently, this goal has been redefined to include narrowing these localizations and cloning specific genes. In the last 5 years, 61 families have participated in this study; 34 have a projected or actual lod score greater than 2.0. Restudy of 12 families reported previously has been a particularly productive aspect of this study and has led to clinical redefinition and new or improved localization of most of these syndromes. Five possible new XLMR syndromes have been identified. Five large families with nonspecific XLMR have been regionally localized. Since many XLMR conditions are based on only 1 or 2 family reports, one of the major purposes of this summary is to provide clinical data on the study families so that collaborative projects can be undertaken with other centers that have similar families.

摘要

本研究的最初目标是定位尽可能多的导致综合征性和非特异性X连锁智力低下(XLMR)的基因。最近,这一目标已重新定义为包括缩小这些定位范围并克隆特定基因。在过去5年中,有61个家庭参与了本研究;其中34个家庭的预期或实际对数优势比(lod score)大于2.0。对先前报告的12个家庭进行重新研究是本研究特别有成效的一个方面,并已导致对大多数这些综合征进行临床重新定义以及新的或改进的定位。已确定了5种可能的新的XLMR综合征。5个患有非特异性XLMR的大家庭已在区域内定位。由于许多XLMR病症仅基于1或2份家庭报告,本综述的主要目的之一是提供有关研究家庭的临床数据,以便能够与拥有类似家庭的其他中心开展合作项目。

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