Mulibrey Nanism is a rare genetic disorder characterized by growth delays, muscle weakness, and various organ abnormalities. It is not contagious as it is caused by mutations in the TRIM37 gene. This condition is inherited in an autosomal recessive manner, meaning both parents must carry a mutated gene for a child to be affected. It is important to consult with a healthcare professional for accurate diagnosis and information.
Mulibrey Nanism is a rare genetic disorder that affects growth and development. It is caused by mutations in the TRIM37 gene. This condition is characterized by severe growth delays, distinctive facial features, and various organ abnormalities.
It is important to note that Mulibrey Nanism is not contagious. It is an inherited condition that is passed down from parents to their children. The disorder follows an autosomal recessive pattern, which means that both parents must carry a mutated copy of the TRIM37 gene for their child to be affected.
Individuals with Mulibrey Nanism have a higher risk of developing certain health complications, such as heart defects, liver disease, and an increased susceptibility to tumors. Early diagnosis and appropriate medical management are crucial in order to address these potential complications and provide the best possible care for affected individuals.
While Mulibrey Nanism is not contagious, it is important to raise awareness about this condition and provide support to affected individuals and their families. Genetic counseling can be beneficial for families with a history of Mulibrey Nanism to understand the risks and make informed decisions about family planning.