Dejerine Sottas Disease is not contagious. It is a rare genetic disorder characterized by progressive nerve damage. The disease affects the peripheral nerves, causing muscle weakness, sensory loss, and impaired coordination. It is inherited in an autosomal recessive manner, meaning both parents must carry the gene mutation for a child to be affected. However, it cannot be transmitted from person to person through contact or exposure.
Dejerine-Sottas disease is a rare genetic disorder that affects the peripheral nerves, causing progressive muscle weakness and sensory loss. It is classified as a type of Charcot-Marie-Tooth disease, which is a group of inherited peripheral neuropathies.
Now, to address the question at hand, Dejerine-Sottas disease is not contagious. It is an inherited condition caused by mutations in certain genes that are involved in the development and maintenance of peripheral nerves. These mutations can be passed down from parents to their children, but the disease itself cannot be transmitted from person to person through any form of contact.
Individuals with Dejerine-Sottas disease typically experience symptoms such as muscle weakness, difficulty walking, loss of sensation, and foot deformities. The severity of the symptoms can vary among affected individuals, even within the same family.
Since Dejerine-Sottas disease is a genetic disorder, it is important for individuals with a family history of the condition to seek genetic counseling and testing if they are planning to have children. Genetic testing can help determine the risk of passing on the disease and allow for informed family planning decisions.
In conclusion, Dejerine-Sottas disease is a non-contagious genetic disorder that affects the peripheral nerves, causing muscle weakness and sensory loss. It is important to raise awareness about this condition and provide support to individuals and families affected by it.