Causes And Risk Factors Of Aarskog Syndrome

Aarskog Syndrome is a rare genetic disorder that causes abnormalities and deformities in the stature, genitalia, facial features, muscles, and bones. While it is more common in men, milder versions of the syndrome can also afflict women. Strong, identifiable symptoms generally present themselves in children by age three. Some of these symptoms are extremely visible, such as wide-set eyes or slanted nostrils, while others may require testing to be discovered, such as the testicles failing to descend into the scrotum. In addition to physical manifestations, Aarskog can delay the onset of sexual maturation. Cognitive development can also be delayed, as the disease impacts the brain.