Aarskog syndrome is a rare genetic condition characterized by short stature and multiple facial, limb and genital abnormalities. Additionally, some types of cognitive disorders may occasionally be present. Up to now, the em FGD1 em gene on the X chromosome is the only gene known to be associated with Aarskog syndrome. Causes of Aarskog Syndrome A mutation of the FGD1 gene, otherwise known as the faciogenital dysplasia 1 gene, is the cause of this syndrome. This gene is located in

Aarskog syndrome is a rare genetic condition characterized by short stature and multiple facial, limb and genital abnormalities. Additionally, some types of cognitive disorders may occasionally be present. Up to now, the em FGD1 em gene on the X chromosome is the only gene known to be associated with Aarskog syndrome. Causes of Aarskog Syndrome A mutation of the FGD1 gene, otherwise known as the faciogenital dysplasia 1 gene, is the cause of this syndrome. This gene is located in
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