![]() ![]() Those adults diagnosed with the condition were interviewed concerning some of the observable symptoms that they had. This involved interviews and observation. The other methods used were primary sources. A detailed analysis of the condition from different authors was readily available, hence enhancing comparison and a deeper understanding of the condition. It was less cumbersome and less time-consuming. ![]() The advantage of this method is that the information was readily available. The secondary sources used include books, journals, and periodicals on MSUD. The methods used in the collection of the data and information in this case study include primary and secondary sources. An individual’s diet should have less branched-chain amino acid (Shellmer, 2010). If not well treated, the patient might show signs of hypoglycemia and acute ketoacidosis. According to Menkes, individuals suffering from this condition should have effective medical care, a checked diet, and have their plasma amino acid levels monitored. This does not, however, prevent neurological deterioration. If the condition is controlled, it can ensure near-normal development, and even reduce the rates of hospitalization. This was established after doing amino acid tests on the blood plasma of the individuals under observation (Donaldson, 2012). According to Donaldson, cerebral edema and metabolic intoxication are the main effects of this condition. As per the findings, dietary measures are more effective in controlling this condition. This was determined by checking the accumulation of the amino acids in the plasma of these two categories of children. ![]() According to some, this condition is hereditary hence children from families that have recorded this condition are more likely to be affected, as opposed to those from MSUD-free families. Various authors have written concerning the MSUD. It was also aimed at determining whether this condition is hereditary (Milunsky, 2011). The case study was done to determine the type of mutation that occurs in the genes of the patients, resulting in this condition. Many individuals with the conditions were observed over a certain period, and laboratory tests were carried out to establish the causes, symptoms, effects and preventive measures. ![]()
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