Skoči na glavni sadržaj

Pregledni rad

https://doi.org/10.26332/seemedj.v1i1.28

Etiology and the Genetic Basis of Intellectual Disability in the Pediatric Population

Višnja Tomac ; Pediatric Clinic, Clinical Hospital Centre Osijek, Osijek, Croatia; Department of Pediatrics, Faculty of Medicine Osijek, Josip Juraj Strossmayer University of Osijek, Osijek, Croatia
Silvija Pušeljić ; Pediatric Clinic, Clinical Hospital Centre Osijek, Osijek, Croatia; Department of Pediatrics, Faculty of Medicine Osijek, Josip Juraj Strossmayer University of Osijek, Osijek, Croatia
Ivana Škrlec ; Department of Medical Biology and Genetics, Faculty of Medicine, Josip Juraj Strossmayer University of Osijek, Osijek, Croatia
Mirna Anđelić ; Department of Medical Biology and Genetics, Faculty of Medicine, Josip Juraj Strossmayer University of Osijek, Osijek, Croatia
Martina Kos ; Pediatric Clinic, Clinical Hospital Centre Osijek, Osijek, Croatia
Jasenka Wagner ; Department of Medical Biology and Genetics, Faculty of Medicine, Josip Juraj Strossmayer University of Osijek, Osijek, Croatia


Puni tekst: engleski pdf 329 Kb

str. 144-153

preuzimanja: 3.117

citiraj


Sažetak

Intellectual disability/mental retardation (ID/MR) is defined as incomplete mental and cognitive development present before the age of 18. There are number of pre-natal and post-natal risk factors that can cause ID/MR but25 %-50% of all have genetic causes. In the general population,the prevalence of ID/MR is about 2 %-3%. Use of standard cytogenetic methods analysis of chromosomes (GTG banding) and FISH (Fluorescent in Situ Hybridization) reveals only a small number of causes, but when usingnew molecular genetics techniques (like chromosomal microarray and next generation sequencing), the rate of causes of ID/MR is increasedand new candidate genes for ID/MR have been discovered. Establishing a diagnosis of ID/MR is important for the patient and it provides genetic counseling for parents.

Ključne riječi

mental retardation; intellectual disability; etiology; submicroscopic chromosome aberrations; genes

Hrčak ID:

186760

URI

https://hrcak.srce.hr/186760

Datum izdavanja:

3.7.2017.

Posjeta: 4.164 *