Serial Killers and The Mind: Predestined or Environmentally Influenced? Serial killers commit more than three murders over a period of time that span about a month. Showsim full cracked screen. For the most part, serial killers commit murder for some sort of psychological benefit (Ramsland, 2013).
Dissociative Identity Disorder Theory Explaining Serial Murder and Murderers Arnon Edelstein Department of Criminology Kaye Academic College, Beersheba, Israel Corresponding Author: Arnon Edelstein Department of Criminology Kaye Academic College Beersheba, Israel Tel: 9104 E-mail: Received June 18, 2015; Accepted August 01, 2015; Published August 08, 2015 Citation: Edelstein A (2015) Dissociative Identity Disorder Theory Explaining Serial Murder and Murderers. J Trauma Treat S4:019. Doi:10.4172/2167-1222.S4-019 Copyright: © 2015 Edelstein A. Hp precisionscan lt software scanjet 4200 c hp printer. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Related article at, Visit for more related articles at.
A study released by the National Academy of Sciences found that 50% of children born in the U.S. Suffer from birth defects, developmental disorders, or are otherwise chronically unhealthy. A government study in Canada also found significant increases in neurological or allergenic developmental disorders over the last 2 decades. Large numbers of peer-reviewed studies have found that the majority of such developmental neurological disorders such as ADD, dyslexia, autism, schizophrenia, other mood disorders, and learning disabilities are primarily caused by prenatal and neonatal exposures to toxic metals or other toxics. Common exposures have been documented for mercury (vaccines, amalgam fillings, and fish), lead (paint, soil, and water fixtures), arsenic (treated wood, pesticides, shellfish, and other foods), aluminum (processed food and pans), cadmium (shellfish, paint, and piping), antimony (Scotch guard), and manganese (soy milk, welding, and metal works). All of these are documented to be extremely neurotoxic. Studies have found that heavy metals, such as mercury, cadmium, lead, aluminum, nickel, and tin, affect chemical synaptic transmission in the brain and the peripheral and central nervous systems.
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They also have been found to disrupt brain and cellular calcium levels that significantly affect many body functions, such as: (a) calcium levels in the brain affecting cognitive development and degenerative CNS diseases and (b) calcium-dependent neurotransmitter release, which results in depressed levels of serotonin, norepinephrine, and acetylcholine—related to mood and motivation. Some factors that have been documented in affective disorders, impulsiveness, and violent behavior are low serotonin levels, abnormal glucose tolerance (hypoglycemia), low folate levels, and low chromium levels, which mercury and other toxic metals have also been found to cause. Toxic metals have also been found to affect cell membrane permeability and thus cellular transfer and levels of other important minerals and nutrients that have significant neurological and health effects, such as magnesium, lithium, zinc, iron, and Vitamins B-6 and B12. Based on thousands of hair tests, at least 20% of Americans are deficient in magnesium and lithium, with zinc deficiencies also common.
The resulting deficiency of such essential nutrients caused by toxic metal exposure has been shown to increase toxic metal neurological damage. Cerebrospinal magnesium was found to be significantly lower in both depression and adjustment disorder and in those who have attempted suicide. A direct mechanism involving mercury’s inhibition of cellular enzymatic processes by binding with the hydroxyl radical (SH) in amino acids appears to be a major part of the connection to these neurological and immune reactive conditions. For example, mercury has been found to strongly inhibit the activity of xanthine oxidase and dipeptyl peptidase (DPP IV), which are required in the digestion of the milk protein casein, and the same protein that is cluster differentiation antigen 26 (CD26), which helps T lymphocyte activation. CD26 or DPPIV is a cell surfact glycoprotein that is very susceptible to inactivation by mercury binding to its cysteinyl domain. Mercury and other toxic metals also inhibit binding of opioid receptor agonists to opioid receptors, while magnesium stimulates binding to opioid receptors.