Causes & Risk Factors Of Fraser Syndrome
Fraser syndrome is a rare genetic disorder. Children born with this gene mutation have webbed or fused fingers and fused eyelids that render them blind. They also have abnormalities of the kidneys, including underdeveloped kidneys that can be unusually small or even absent. The child may lack one or both kidneys. They also have abnormalities of the genitals including undescended testicles, abnormal urinary openings, deformed fallopian tubes, or a bicornate uterus, which means the uterus, instead of being pear-shaped, has two horns. The vaginal labia may also be fused. Doctors diagnose Fraser syndrome through a medical exam, a medical history of the family, and by imagining tests such as computerized tomography (CT) scans. Get to know the causes and risk factors of Fraser syndrome now.