A Comparison of Intelligence Quotient in Children with and without beta-Thalassemia Major

被引:0
作者
Meymandi, Samaneh Homayouni [1 ]
Seyednezhad-Golkhatmi, Seyed Hamid [2 ]
Meymandi, Mandana Homayouni [3 ]
机构
[1] Zahedan Univ Med Sci, Dept Psychol, Zahedan, Iran
[2] Univ Social Welf & Rehabil Sci, Dept Psychol, Tehran, Iran
[3] Shiraz Univ, Dept Psychol, Shiraz, Iran
来源
GALEN MEDICAL JOURNAL | 2015年 / 4卷 / 04期
关键词
Thalassemia; beta-Thalassemia; Intelligence Quotient; Cognitive Function; Children;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Thalassemia is the most common hemoglobinopathy worldwide. Children with beta-thalassemia major have several risk factors for cognitive problems. The aim of this study is to evaluate intelligence quotient in children with beta-thalassemia major and healthy counterparts using Wechsler Intelligence Scale. Materials and Methods: Within a case-control design and using convenience sampling method, the present study was carried out in Zahedan and Shiraz in 2012. Participants were matched based on their age, gender and city of residence (40 children with beta-thalassemia major and 40 healthy children aging 6 to 12 years. Wechsler Intelligence Scale Revised (WISC-R) was used to find the participants' Verbal Performance and Full intelligence scores. The scores of the two groups were then compared using descriptive analysis and independent t-test. Results: As compared with their healthy counterparts, children with beta-thalassemia major had lower scores on both Verbal Scale and Full Scale (P<0.01); however, the difference between the two groups' scores on Performance Scale fell short of significance. Conclusions: Intelligence decline does not necessarily occur in children with beta-thalassemia. They are just slightly lower than their healthy counterparts and they need to receive more attention in education in order to improve.
引用
收藏
页码:132 / 138
页数:7
相关论文
共 26 条
[1]  
Atiq M., 2006, SMJ Singapore Medical Journal, V47, P693
[2]   Psychosocial burden of β-thalassaemia major in Antalya, south Turkey [J].
Canatan, D ;
Ratip, S ;
Kaptan, S ;
Cosan, R .
SOCIAL SCIENCE & MEDICINE, 2003, 56 (04) :815-819
[3]   Auditory and visual toxicity during deferoxamine therapy in transfusion-dependent patients [J].
Chen, SH ;
Liang, DC ;
Lin, HC ;
Cheng, SY ;
Chen, LJ ;
Liu, HC .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2005, 27 (12) :651-653
[4]   Neurocognitive function in patients with β-thalassemia major [J].
Duman, Ozgur ;
Arayici, Sema ;
Fettahoglu, Cigil ;
Eryilmaz, Nurkan ;
Ozkaynak, Sibel ;
Yesilipek, Akif ;
Hazar, Volkan .
PEDIATRICS INTERNATIONAL, 2011, 53 (04) :519-523
[5]   Neurophysiologic and intellectual evaluation of beta-thalassemia patients [J].
Economou, M ;
Zafeiriou, DI ;
Kontopoulos, E ;
Gompakis, N ;
Koussi, A ;
Perifanis, V ;
Athanassiou-Metaxa, M .
BRAIN & DEVELOPMENT, 2006, 28 (01) :14-18
[6]   Beta-thalassemia [J].
Galanello, Renzo ;
Origa, Raffaella .
ORPHANET JOURNAL OF RARE DISEASES, 2010, 5
[7]   Focal neurological deficits in children with β-thalassemia major [J].
Incorpora, G ;
Di Gregorio, F ;
Romeo, MA ;
Pavone, P ;
Trifiletti, RR ;
Parano, E .
NEUROPEDIATRICS, 1999, 30 (01) :45-48
[8]  
Karimi M, 2006, SAUDI MED J, V27, P982
[9]   The molecular analysis of β-thalassemia mutations in Lorestan Province, Iran [J].
Kiani, Ali Asghar ;
Mortazavi, Yousef ;
Zeinali, Sirous ;
Shirkhani, Yaghob .
HEMOGLOBIN, 2007, 31 (03) :343-349
[10]   Diagnostic approach to hemoglobinopathies [J].
Kutlar, Ferdane .
HEMOGLOBIN, 2007, 31 (02) :243-250