X-Linked intellectual disability update 2022

被引:10
作者
Schwartz, Charles E. [1 ]
Louie, Raymond J. [1 ]
Toutain, Annick [2 ]
Skinner, Cindy [1 ]
Friez, Michael J. [1 ]
Stevenson, Roger E. [1 ]
机构
[1] Greenwood Genet Ctr, 113 Gregor Mendel Circle, Greenwood, SC 29646 USA
[2] Ctr Hosp Univ, Dept Med Genet, Tours, France
关键词
genes; intellectual disability; X-chromosome; MENTAL-RETARDATION GENE; OSTEOPATHIA STRIATA CONGENITA; LINKAGE ANALYSIS; REGIONAL LOCALIZATION; GROWTH-RETARDATION; FUNCTIONAL DISOMY; SHORT STATURE; FMR1; GENE; MRX GENE; DUPLICATION;
D O I
10.1002/ajmg.a.63008
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genes that are involved in the transcription process, mitochondrial function, glycoprotein metabolism, and ubiquitination dominate the list of 21 new genes associated with X-linked intellectual disability since the last update in 2017. The new genes were identified by sequencing of candidate genes (2), the entire X-chromosome (2), the whole exome (15), or the whole genome (2). With these additions, 42 (21%) of the 199 named XLID syndromes and 27 (25%) of the 108 numbered nonsyndromic XLID families remain to be resolved at the molecular level. Although the pace of discovery of new XLID genes has slowed during the past 5 years, the density of genes on the X chromosome that cause intellectual disability still appears to be twice the density of intellectual disability genes on the autosomes.
引用
收藏
页码:144 / 159
页数:16
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