Aarskog Syndrome

Aarskog syndrome is a rare genetic disorder that affects the development of several parts of the body, especially height, facial features, hands and, in males, the genitals.

Associated features: It can be accompanied by short stature, wide spacing between the eyes, short fingers and other physical details that are identified during growth.

Origin: It is an inherited alteration that is usually passed on through the X chromosome, so it mainly affects boys.

Who to consult? The pediatrician is the one who follows the child's growth and, in the presence of features that suggest a genetic syndrome, requests the opinion of medical genetics. If you notice an unusual pattern in your child's development, it is worth discussing it with a professional for appropriate guidance.