Kowsar Gene Cell Tissue 2345-6833 5 4 2018 12 26 10.5812/gct.84401 Negin Parsamanesh Student Research Committee, Birjand University of Medical Sciences, Birjand, Iran. Ebrahim Miri-Moghaddam 2. Cardiovascular Diseases Research Center & Department of Molecular Medicine, School of Medicine, Birjand University of Medical Sciences, Birjand, Iran, Ebrahim Miri-Moghaddam, Ph. D in Human Molecular Genetics Cardiovascular Diseases Research Center, Birjand University of Medical Sciences, Birjand, Iran. E-mail: moghaddam4@yahoo.com- or miri4@Bums.ac.ir Tel: +98-5633381230, Fax: +98-5633295811 Review Article 2018 12 18 2018 9 18 2018 12 26 2018 10 31 : Intellectual disability or cognitive disturbance is a prevalent neurological problem determined by the low-level intelligence quotient (< 70). Intellectual disability affects approximately 1% to 3% of the general population. The collaboration of environmental factors and heterogeneous genetic agents can be a cause of intellectual disability in X-linked, autosomal dominant, recessive, and inheritance of mitochondria patterns. Spontaneous mutations in germ line may have vital phenotypic outcomes when involved in bases of the whole genome. Discovering the etiology of intellectual disability plays a role in precise diagnosis and can help the couple plan in the near future. Development of genome sequencing can improve mutation detection in a single experiment. These tools have been shown as a new way for the conception of the molecular pathway in a genetic disorder. This finding can have a profound implication for early diagnosis and treatment development. This study reviewed recent reports of de novo mutations detection of intellectual disability in the Iranian population by whole exome sequencing approaches. http://genecelltissue.com/en/articles/84401.html https://neoscriber.org/cdn/dl/193a4488-12ba-11e9-aa7d-5f831f16c472