How are Mendelian Disorders Diagnosed?
Mendelian illnesses can be diagnosed by a variety of approaches. One of the more popular ways to diagnose chromosomal abnormalities or gene mutations is through DNA testing. A Mendelian disorder risk assessment is another service offered by genetic counselors. It may be possible to determine people who may be at a higher risk of acquiring a Mendelian condition by looking at their family history. Moreover, certain Mendelian diseases like cystic fibrosis and sickle cell anemia can be identified by blood tests.
Mendelian Disorder in Human
Mendelian disorders are a form of genetic disorder that is caused by the inheritance of single or multiple mutant genes from one or both parents. The function of the mutant gene determines how severe a Mendelian disorder is. The condition is typically severe if the gene controls a crucial function. Mendelian diseases include, for instance, Tay-Sachs disease, sickle cell anemia, and cystic fibrosis. These illnesses can be fatal and range in severity from mild to severe.