identification of chromosome abnormalities in subtelomeric regions using multiplex ligation dependent probe amplification (mlpa) technique in 100 iranian patients with idiopathic mental retardation

materials and methods a number of 100 patients with imr, normal karyotypes and negative fragile-x and metabolic tests were screened for subtelomeric abnormalities using mlpa technique. results nine of 100 patients showed subtelomeric abnormalities with at least one of the two mlpa kits. deletion in a single region was found in 3 patients, and in two different subtelomeric regions in 1 patient. duplication was only single and was present in 2 patients. three patients were found to have both a deletion and duplication.mlpa testing in the parental samples of 7 patients which was accessible showed that 4 patients were de novo, 2 patients had inherited from a clinically normal mother, and one had inherited from a clinically normal father. screening with the two mlpa kits (salsa p036 and salsa p070) proved abnormality in only five of the 9 patients. conclusions so, the prevalence rate of abnormal subtelomeres using mlpa technique in patients with idiopathic mr in our study was 5 - 9%, the higher limit referring to the positive results of one of the two mlpa kits, and the lower limit representing the results of positive double-checking with the two mlpa kits. background mental retardation/developmental delay (mr/dd) is present in 1 - 3% of the general population (1, 2). mr is defined as a significant impairment of both cognitive (iq < 70) and social adaptive functions, with onset before 18 years of age. objectives the purpose was to determine the results of subtelomeric screening by the multiplex ligation dependent probe amplification (mlpa) technique in 100 selected patients with idiopathic mental retardation (imr) in iran.