X-Linked intellectual disability update 2022

被引:16
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
相关论文
共 126 条
[1]  
Ahmad W, 1997, AM J HUM GENET, V61, pA265
[2]  
Akiyama M, 2001, AM J MED GENET, V99, P111, DOI 10.1002/1096-8628(2001)9999:9999<::AID-AJMG1150>3.0.CO
[3]  
2-C
[4]   Pathogenic Variants in GPC4 Cause Keipert Syndrome [J].
Amor, David J. ;
Stephenson, Sarah E. M. ;
Mustapha, Mirna ;
Mensah, Martin A. ;
Ockeloen, Charlotte W. ;
Lee, Wei Shern ;
Tankard, Rick M. ;
Phelan, Dean G. ;
Shinawi, Marwan ;
de Brouwer, Arjan P. M. ;
Pfundt, Rolph ;
Dowling, Cari ;
Toler, Tomi L. ;
Sutton, V. Reid ;
Agolini, Emanuele ;
Rinelli, Martina ;
Capolino, Rossella ;
Martinelli, Diego ;
Zampino, Giuseppe ;
Dumic, Miroslav ;
Reardon, William ;
Shaw-Smith, Charles ;
Leventer, Richard J. ;
Delatycki, Martin B. ;
Kleefstra, Tjitske ;
Mundlos, Stefan ;
Mortier, Geert ;
Bahlo, Melanie ;
Allen, Nicola J. ;
Lockhart, Paul J. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2019, 104 (05) :914-924
[5]   Mapping of MRX81 in Xp11.2-Xq12 suggests the presence of a new gene involved in nonspecific X-linked mental retardation [J].
Annunziata, I ;
Lanzara, C ;
Conte, I ;
Zullo, A ;
Ventruto, V ;
Rinaldi, MM ;
D'Urso, M ;
Casari, G ;
Ciccodicola, A ;
Miano, MG .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2003, 118A (03) :217-222
[6]   Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders [J].
Aref-Eshghi, Erfan ;
Kerkhof, Jennifer ;
Pedro, Victor P. ;
DI France, Groupe ;
Barat-Houari, Mouna ;
Ruiz-Pallares, Nathalie ;
Andrau, Jean-Christophe ;
Lacombe, Didier ;
Van-Gils, Julien ;
Fergelot, Patricia ;
Dubourg, Christele ;
Cormier-Daire, Valerie ;
Rondeau, Sophie ;
Lecoquierre, Francois ;
Saugier-Veber, Pascale ;
Nicolas, Gael ;
Lesca, Gaetan ;
Chatron, Nicolas ;
Sanlaville, Damien ;
Vitobello, Antonio ;
Faivre, Laurence ;
Thauvin-Robinet, Christel ;
Laumonnier, Frederic ;
Raynaud, Martine ;
Alders, Marielle ;
Mannens, Marcel ;
Henneman, Peter ;
Hennekam, Raoul C. ;
Velasco, Guillaume ;
Francastel, Claire ;
Ulveling, Damien ;
Ciolfi, Andrea ;
Pizzi, Simone ;
Tartaglia, Marco ;
Heide, Solveig ;
Heron, Delphine ;
Mignot, Cyril ;
Keren, Boris ;
Whalen, Sandra ;
Afenjar, Alexandra ;
Bienvenu, Thierry ;
Campeau, Philippe M. ;
Rousseau, Justine ;
Levy, Michael A. ;
Brick, Lauren ;
Kozenko, Mariya ;
Balci, Tugce B. ;
Siu, Victoria Mok ;
Stuart, Alan ;
Kadour, Mike .
AMERICAN JOURNAL OF HUMAN GENETICS, 2020, 106 (03) :356-370
[7]   LINKAGE ANALYSIS SUGGESTS AT LEAST 2 LOCI FOR X-LINKED NON-SPECIFIC MENTAL-RETARDATION [J].
ARVEILER, B ;
ALEMBIK, Y ;
HANAUER, A ;
JACOBS, P ;
TRANEBJAERG, L ;
MIKKELSEN, M ;
PUISSANT, H ;
PIET, LL ;
MANDEL, JL .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1988, 30 (1-2) :473-483
[8]  
BarDavid S, 1996, AM J MED GENET, V64, P83, DOI 10.1002/(SICI)1096-8628(19960712)64:1<83::AID-AJMG15>3.0.CO
[9]  
2-O
[10]   Evidence for Increased SOX3 Dosage as a Risk Factor for X-Linked Hypopituitarism and Neural Tube Defects [J].
Bauters, Marijke ;
Frints, Suzanna G. ;
Van Esch, Hilde ;
Spruijt, Liesbeth ;
Baldewijns, Marcella M. ;
de Die-Smulders, Christine E. M. ;
Fryns, Jean-Pierre ;
Marynen, Peter ;
Froyen, Guy .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2014, 164 (08) :1947-1952