Genetic basis for developmental delay/mental retardation

被引:0
作者
Barisic, Ingeborg [1 ]
Della Marina, Branka Marusic [2 ]
机构
[1] Klin Djecje Bolesti Zagreb, Referentni Ctr Ministarstva Zdravstva Pracenje Ko, Zagreb 10000, Croatia
[2] Poliklin Neuron, Zagreb, Croatia
关键词
mental retardation; genetics; diagnosis; developmental disabilities; dignosis; cytogenetic analysis; molecular diagnostic techniques; chromosome aberrations; COMPARATIVE GENOMIC HYBRIDIZATION; LINKED MENTAL-RETARDATION; FRAGILE-X-SYNDROME; DEPENDENT PROBE AMPLIFICATION; RETT-SYNDROME PATIENTS; COPY NUMBER CHANGES; ARRAY-CGH; MECP2; GENE; SUBTELOMERIC REARRANGEMENTS; MICROARRAY ANALYSIS;
D O I
暂无
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Although developmental delay/mental retardation is a common disorder, the causes remain unknown in about half of the cases. In recent years advances in molecular cytogenetics and molecular genetics have shown that submicroscopic genome abnormalities are a frequent, until now under-recognized cause of mental retardation. The use of new techniques allows recognition of the known clinical entities as well as definition of new disorders. We review today's achievements in this field in the context of recommendations for the rational use of diagnostic procedures in the evaluation of the genetic causes of developmental delay/mental retardation in clinical settings.
引用
收藏
页码:191 / 200
页数:10
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