Acromicric Dysplasia is a rare genetic disorder characterized by skeletal abnormalities and short stature. It is not contagious and cannot be transmitted from person to person. This condition is caused by mutations in the ACAN gene, which is responsible for producing a protein involved in the development of bones and cartilage. Acromicric Dysplasia is typically inherited in an autosomal dominant manner, meaning that an affected individual has a 50% chance of passing the condition on to their children.
Acromicric Dysplasia is a rare genetic disorder that affects bone and cartilage development. It is characterized by short stature, distinctive facial features, and skeletal abnormalities. This condition is caused by mutations in the ACAN gene, which provides instructions for producing a protein called aggrecan.
It is important to note that Acromicric Dysplasia is not contagious. It is an inherited condition, meaning it is passed down from parents to their children through genetic mutations. The mutations in the ACAN gene can occur spontaneously or be inherited from one or both parents who carry the mutated gene.
Individuals with Acromicric Dysplasia may experience various symptoms, including short stature, joint stiffness, limited joint mobility, and distinctive facial features such as a round face, a small nose, and a prominent forehead. However, the severity of symptoms can vary among affected individuals.
Diagnosis of Acromicric Dysplasia is typically made through clinical evaluation, genetic testing, and imaging studies. While there is no cure for this condition, management focuses on addressing specific symptoms and providing supportive care.
In conclusion, Acromicric Dysplasia is a non-contagious genetic disorder that affects bone and cartilage development. It is important to consult with a healthcare professional for accurate diagnosis and appropriate management strategies.