Leri Pleonosteosis is a rare genetic disorder characterized by abnormal bone development. It is not contagious and cannot be transmitted from person to person. The condition is caused by mutations in the COMP gene and is inherited in an autosomal dominant manner. Leri Pleonosteosis affects the skeletal system, causing various skeletal abnormalities. It is important to consult with a healthcare professional for accurate diagnosis and management of this condition.
Leri Pleonosteosis is a rare genetic disorder that affects the bones and connective tissues. It is also known as Leri-Weill dyschondrosteosis or LWD. This condition is caused by mutations in the SHOX gene, which plays a crucial role in bone development.
Now, to answer your question, Leri Pleonosteosis is not contagious. It is an inherited condition, meaning it is passed down from parents to their children through genetic mutations. It is important to note that this disorder is not caused by any infectious agent or external factors.
Individuals with Leri Pleonosteosis may experience various symptoms, including short stature, skeletal abnormalities, and joint deformities. These symptoms can vary in severity from person to person. Diagnosis is typically made through a combination of physical examination, medical history, and genetic testing.
Since Leri Pleonosteosis is a genetic disorder, it cannot be transmitted from one person to another through contact or exposure. It is important to provide support and understanding to individuals with this condition, as they may face challenges related to their physical appearance and mobility.
Although Leri Pleonosteosis is not contagious, it is always recommended to consult with healthcare professionals for accurate information and guidance regarding this condition.