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Why is it called Kennedy's disease?

Published in Medical Conditions 2 mins read

Kennedy's disease, also known as spinal and bulbar muscular atrophy (SBMA), is named after Joseph P. Kennedy Jr., the son of Joseph P. Kennedy Sr. and Rose Kennedy. He was the older brother of John F. Kennedy, Robert F. Kennedy, and Edward M. Kennedy.

Joseph P. Kennedy Jr. died in World War II, but his family continued to be affected by the disease. His younger brother, Robert F. Kennedy, was diagnosed with Kennedy's disease in the 1960s, and his symptoms eventually led to his death in 1968.

While the disease was first described in the 1960s, it was not until the 1990s that the gene responsible for Kennedy's disease was identified. The gene is called androgen receptor (AR), and mutations in this gene cause the disease.

Kennedy's disease is a rare, inherited disorder that affects the muscles. It is characterized by progressive weakness and atrophy of the muscles, particularly in the arms and legs. It can also affect the muscles that control swallowing and breathing.

The disease is named after the Kennedy family because of its association with the family. However, it is important to note that Kennedy's disease is not unique to the Kennedy family. It is a rare disease that can affect anyone, regardless of their family history.

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