Attention Deficit Hyperactivity Disorder (ADHD) and Its Origin

Nikolas and Burt argue that “Attention Deficit Hyperactivity Disorder (ADHD) is one of the common disorders affecting small children and can continue through adulthood”. Some of the common symptoms associated with this disorder include hyperactivity and behavioral problems. The patient might sometimes be unable to pay attention. The “three subtypes of this condition include combined hyperactive-impulsive, predominantly inattentive, and predominantly hyperactive-impulsive.” The cause of this condition has been debated for several decades. Modern scientists are also unsure of the major causes of ADHD. However, numerous studies have indicated that human genes play a significant role in the development of this disorder. This fact explains why numerous studies are being conducted in order to understand the risk factors and causes of this condition.

Some scientists believe strongly that ADHD should be classified as a genetic disorder. This is the case because the condition is common in specific families. Studies of twins have also indicated that the disorder is common in different families. This understanding has, therefore, encouraged medical practitioners and scientists to examine various genes that might be associated with this condition. Studies show clearly that ADHD is a genetic condition. That being the case, new studies will be critical in supporting the health needs of the affected persons. Scientists should also conduct new studies and experiments in order to identify the significant genes associated with this condition. Doctors can also “use this knowledge to control the condition before it produces new complications.” This knowledge will make it easier for many practitioners to offer appropriate treatment regimes for ADHD.

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