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This research is conducted to achieve two objectives. First, study of clinical suitability and diagnostic precision in paraclinical experiments and study of biochemical factors in the diagnosis of AD/HD and second, study of the effectiveness of blood tests in identification of iron panel factors, study of blood mercury level, study of SE in AD/HD and comparing it with control group (normal children). At the first stage of the study, after analysis by QEEG, all factors to be tested underwent paraclinical experiments. The diagnostic precision of QEEG is estimated at 94%. The results of the first stage demonstrated that the paraclinical experiments are an effective tool with a high diagnostic precision for the diagnosis of AD/HD. The results of the second stage of study demonstrated that both groups suffer from iron deficiency anemia and there is no significant relationship between development of AD/HD symptoms and the iron deficiency anemia. Also the blood Ferritin in the tested group was higher than that of control group. Statistically, no significant relationship was noted between the CBC and development of AD/HD symptoms, yet a significant relationship was observed between reduction of Hb level and development of AD/HD symptoms. It was also concluded that SE stool infection in AD/HD children was higher than that of normal children. In children with AD/HD, vitamin B was less than that of normal children and there was significant relationship between increase in the mercury level of blood and development of attention and concentration deficit disorder (AD/HD).

current research journal of biological sciences

Comparison between QEEG as a Neurofeedback Tool to Diagnose AD/HD Disorder and Hematological-biochemical Para-clinical Indicators on Children with AD/HD Disorder and Children without Such Symptoms