Some rare genetic disorders are known to be inherited through families and history. Some of these, like cystic fibrosis and sickle cell anemia are rare and have high mortality rates. Although these disorders are not considered life-threatening in most cases, they can lead to death within a short time. Research on the causes of these disorders has not been conclusive enough to identify the exact causes of each disorder, but it has been studied extensively and the list of possible diagnoses is long. Researchers are primarily interested in finding a cure for the disorder and not the causes.
Researchers are involved in researching rare diseases because they pose a serious threat to public health. Most people are unaware that rare diseases exist. Genetic Research is crucial in order to save the public from such hazards. The ultimate aim is to prevent further deterioration of public health.
Research in the field of genetic disorders is highly dependent on the type of disorder studied. There are diseases that are commonly associated with a particular ethnic group, like Type 1 Diabetes. The researchers must therefore collect sufficient data from samples belonging to different ethnic groups in order to study ethnic differences in susceptibility. This research can help find methods of prevention and treatment of diabetes and other genetic disorders. Similarly, research into the causes of acquired mental retardation can also help develop methods of preventing this disease among future generations.
The scientists conducting a research into rare genetics should be vigilant about collecting adequate samples from patients with such disorders. Failure to do so would lead to invalid research results. All parts of the body must be taken for research, including the scalp, finger tips, and fingernails. These cells can be used to study different types of cells, such as muscle and blood cells.
Some research areas are focusing more on rare genetics affecting humans. In the case of research into Rare Genetics diseases affecting animals, researchers must also collect sufficient samples from animals belonging to different species. Similarly, rare genetic disorders affecting plants and microorganisms need to be studied from plant cells, soil and marine samples. The entire range of rare genetics is now becoming available to study even microorganisms, such as bacteria and yeasts.
Research into rare genetics is important because it allows us to discover new drugs that can fight genetic disorders. The resistance against some common diseases has caused difficulties for researchers to produce effective medicines. Researchers are also able to learn about rare genetic mechanisms involved with the treatment of these conditions by working hard to create effective medicines. Apart from this, there is another important reason behind conducting research on rare diseases. Rare genetic disorders may provide clues to better treatment options for common diseases.
Rare genetic disorders research can help find out more about inherited conditions, like Down syndrome, Turner's syndrome, Huntington's disease, polycystic kidney disease, sickle cell anemia etc. These disorders can be passed on from one parent to the other. It is estimated that more than half of all genetic disorders have some variant found only in one generation. Hence, conducting research on genetic disorders will help develop new treatments.
There are different types of rare genetic disorders. Some are rare while others are more common. For example, the DNA hybridization is a research method used to analyze rare genetic conditions. Allely's disease is another rare genetic disorder. It affects blood cells and results a red blood cell disorder. Studies on rare diseases are still in their infancy. This field is still in its infancy, but it is expected that researchers will soon discover the entire genetic mechanism behind genetic disorders.
