Discusses of the Adams-Oliver Disorder Essay

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The Adams-Oliver disorder is a rare disease that is characterized by aplasia cutis congenital and limb defects. Many patients with this disorder have problems with the heart, nerves, and skin. It may affect various structures of the whole organism; most cases of the disease referred to an autosomal prevailing feature. This autosomal attribute might be sent from parents and connected with their genes; it also means that for the disorder to manifest, one parent with the mutated gene can have the condition. It is essential to scrutinize relevant information about the disease to understand its features and peculiarities.

One more vital fact was mentioned; the Adams-Oliver disorder is not affected by gender and race. Moreover, the disease is not expressed if the person is a carrier of autosomal recessive inheritance. People may have inclinations of various types, and the illness might spread out of families. Some scientists suggested that the disorder develops at the embryonic stage when some abnormalities in the vascular system (Dudoignon et al., 2019). There are no possibilities to hold tests and pre-analyses of the disease, as the location of the affected gene is not fully discovered and understood. For this reason, the Adams-Oliver disorder is not treatable; there is no clear understanding of the illness. It is crucial to managing the condition through a proper multidisciplinary approach, as the illness requires a muscular cure. It is also learned that currently, it is possible to ease and hold effects back, but not treatment.

Overall, the Adams-Oliver disorder is a complicated issue that should be studied and explored. It affects limbs, the nervous system, and processes within the organism. Unfortunately, there is a high mortality chance in people with this disease. New mutations of the affected gen may appear and generate new forms of the disorder. Therefore, it should be visualized to provide medicals with a complete understanding of the disorder and treatment abilities.

Reference

Dudoignon, B., Huber, C., Michot, C., di Rocco, F., Girard, M., Lyonnet, S., Rio, M., Rabia, S. H., Daire, V. C., & Baujat, G. (2019). . American Journal of Medical Genetics Part A, 182(1), 29–37.

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