Arthrogryposis multiplex congenita - what does this mean
Arthrogryposis multiplex congenita is a rare, non-progressive disorder that is present at birth and characterized by multiple joint contractures, which are caused by lack of movement in the womb due to muscle weakness or abnormal development. it can affect any part of the body, but is most common in the arms and legs. it is believed to be caused by genetic and environmental factors, and can be associated with other medical conditions.
What happens during the disease - arthrogryposis multiplex congenita
Arthrogryposis multiplex congenita is a rare disorder that is caused by a combination of genetic and environmental factors. it is characterized by a lack of movement in multiple joints due to abnormal development of the muscles, tendons, and ligaments. the exact cause of this disorder is unknown, but it is believed to be related to a disruption in the normal development of the fetal muscles and connective tissue during the early stages of pregnancy. this disruption can be due to genetic mutations, environmental factors, or a combination of both.
Arthrogryposis multiplex congenita - Prevention
Arthrogryposis multiplex congenita can be prevented by avoiding certain risk factors, such as maternal infections during pregnancy, exposure to certain medications or toxins, and genetic abnormalities. women should receive appropriate prenatal care to reduce the risk of infections and other complications. women should also be aware of the potential risks associated with certain medications or toxins and discuss them with their healthcare provider. genetic counseling may be beneficial for families with a history of the condition.