ACvoiman
ACVOiman is a rare genetic disorder characterized by increased levels of acid phosphatase in the blood. The condition is typically inherited in an autosomal dominant pattern, meaning a single copy of the mutated gene is sufficient to cause the disorder.
Symptoms of ACVOiman can vary in severity and may include a range of physical and medical issues.
The underlying cause of ACVOiman is a mutation in the PHEX gene. This gene normally codes for
Diagnosis of ACVOiman typically involves a combination of laboratory tests, including blood work and imaging studies.
While ACVOiman is a rare condition, research into its underlying causes and complications has provided new
In addition to the PHEX mutation, scientists have also identified mutations in other genes that may contribute
Overall, while ACVOiman can cause significant health problems, prompt diagnosis and treatment can help manage symptoms