Human Immunodeficiency Virus (HIV), a neurotropic infection, quickly attacks the mind following contamination. HIV repeats in the mind in an unobtrusive number of astrocytes, microglia, and macrophages, prompting provocative and neurotoxic host reactions. The expression "HIV-Related Neurocognitive Infections" alludes to serious neurological diseases welcomed on by HIV Associated Neurocognitive Disorder (HAND). The advancement of unusually low degrees of engine coordination, concentration, and memory are signs of HAND. From Asymptomatic Neurocognitive Debilitation (ANI), gentle neurocognitive issue, HIV-associated Motor Neuron Disease (MND), to the most extreme Hiv Related Dementia (HAD), HAND has various clinical appearances. The essential driver of HAND and the most pervasive neurologic condition influencing the mind in those tainted with HIV-1 is Hiv Encephalitis (HIVE). There are nine fundamental hereditary subtypes of HIV-1, which are separated into three gatherings (M, O, and N) and show boundless hereditary variety. In excess of 86% of the flowing HIV-1 varieties have a place with clades B and C. Clade C of the HIV-1 infection is more pervasive in Southern and East Africa, India, and Nepal than clade B, which prevails in North America, Western Europe, and Australia (liable for around half of all HIV diseases). As indicated by reports, clade B of HIV-1 is more neuropathogenic than clade C. Around 20%-30% of individuals with cutting-edge HIV-1 clade B contamination displayed HAD side effects before the inescapable utilization of Exceptionally Antiretroviral Treatment (HAART).
