
CYTOGENETIC FINDINGS IN MENTALLY
RETARDED IRANIAN PATIENTS Nasiri F1, Mahjoubi F1,2,*, Manouchehry F1, Razazian F1, Mortezapour F1, Rahnama M1 *Corresponding Author: Dr. Frouzandeh Mahjoubi, Genetics Department, Iran Blood Transfusion Organization
Research Centre, High Institute for Research and Education in Transfusion Medicine, Hemmat Express Way, Next to
the Milad Tower, Tehran, Iran; Tel.: +9821-44580389; Fax: +9821-44580399; E-mail: Frouz@ nigeb.ac.ir page: 29
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INTRODUCTION
Mental retardation (MR) is characterized by destruction
in intellectual abilities, and by an inability
to adapt to the environment and the social situation.
Mental retardation is found in individuals either as an
isolated finding, or as part of an underlying disorder
[1]. The worldwide prevalence of MR is about 2.3%
[2]. Despite large studies being conducted to discover
the etiology of MR, in less than 50% of MR cases is
the cause identified and the genetic defect known to
be responsible for 17-47% of MR cases [3].
It is known that numerical and structural chromosomal
anomalies are one of the most common
causes of MR seen in these patients [4-12]. Identification
of the causes of MR in a patient is of great
importance because of the consequences it has for the
prognosis, risk of occurrence in other family members,
and prevention. Mental retardation is the reason
for a substantial portion of referrals of patients and
families to the genetic counseling unit. Here we summarize
the result of a cytogenetic study performed on
865 mentally retarded Iranian patients consecutively
referred to the Cytogenetics Department of the Iran
Blood Transfusion Organisation (IBTO) Research
Centre, Tehran, Iran.
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