Genetic or Hereditary Conditions are disorders caused by abnormalities in an individual’s DNA, which can be passed down from one generation to the next. These conditions may arise from mutations in specific genes, chromosomal abnormalities, or inherited genetic traits. Depending on the condition, symptoms can range from mild to severe and may affect various systems in the body. In some cases, a genetic disorder may be present at birth, while in others, symptoms may develop later in life. Treatment options vary based on the specific condition but often include medications, therapies, and in some cases, surgery. 

Many people with genetic or hereditary conditions, like Marfan’s Syndrome, describe it as a deeply unique physical adjustment or challenge. Marfan’s Syndrome is a condition that affects the connective tissues, and people with Marfan’s Syndrome are also distinctive in that they tend to be tall and thin, with long legs, arms, and fingers. While not everyone with a lanky appearance has Marfan’s Syndrome, people with this condition tend to have narrow frames. The expressions of Marfan’s Syndrome can also vary from person to person. For instance, one person with Marfan’s Syndrome might have more problems with their heart, while another person with the condition might not have heart problems but have severe problems with their sight. Getting a medical diagnosis will also be necessary to determine whether a person has Marfan’s Syndrome. 

A disabling condition does not need to be disabling every day to support a finding that a person is unable to work because being able to work means doing it daily, week after week, on a regular and continuous basis.