Biological Explanations of Abnormality

639 Words3 Pages
According to the biological model, there are a few biological things that explain abnormalities; genetics, brain damage, infections, biochemistry and neuroanatomy. The biological model states that some people might be genetically at risk of developing a mental disorder. However, there is only evidence for this in the cases of bipolar disorder and schizophrenia. For example, first degree relatives are more likely to develop schizophrenia than second degree relatives. Gottesman & Shield (1972) found that concordance rate for schizophrenia in non-identical twins is approximately 9% whereas for identical twins, the concordance rate is 42%. This supports the biological model as if schizophrenia had nothing to do with a persons gene, the other twin might not have developed schizophrenia. Also, through ‘gene mapping’, Meyer (2001) found that a mutation in a gene called WKL1 was found I people with a particular form of schizophrenia. Brain damage may also be to blame for abnormalities. For example, excessive alcohol and drug abuse can damage the brain and may result in hallucinations or symptoms of mental health disorders such as Korsakoff’s syndrome. Case studies such as that of Clive Wearing also support the biological model as Clive Wearing had a brain injury and so did not have a long short term memory span yet he could remember how to do procedural tasks such as playing the piano. A weakness of this support is that Clive Wearing is a specific case and can not, therefore, be generalised to other individuals. The biological model also states that infections can affect the normality of an individual. Crow (1984) proposed that schizophrenia is caused by a retrovirus which becomes incorporated into a person’s DNA. Research suggests that some disorders such as schizophrenia may be linked to exposure to certain viruses while still in the womb. Torrey (2001) found that
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