Treatment Options For Fraser Syndrome

Fraser syndrome is a medical condition caused by a rare genetic disorder. The signs are the webbing of the fingers and toes, kidney abnormalities, and fusion of the eyelids. Those affected can also have kidney dysfunctions, including underdeveloped or missing kidneys. Infants are born with this condition, and it is diagnosed at birth. The main indicators are the physical malformations on the body. This condition occurs when there is a mutant gene present during the time of conception. Get to know how Fraser syndrome is treated now.

Corrective Surgery

Fraser syndrome causes many malformations in the body that affects the nose, fingers, toes, and reproductive organs. Each defect has an impact on the infant's health and wellbeing and needs to be addressed, so the child can have a better quality of life. Since the eyelids become totally fused and deformed, the infant's eyes are closed shut. The skin can pass from the forehead and onto the cheek with a malformed eye underneath. This condition is called cryptophthalmos and leads to blindness because the cornea cannot develop properly, and the eyes are covered by skin.

The children with this congenital anomaly typically need to undergo corrective surgery to enhance their eyesight. There are surgeries performed to correct the closed eyelids that improve vision in children. During this surgery, the cornea is protected, and the upper and lower eyelids are separated and reconstructed. Skilled oculoplastic surgeons do this procedure to provide children with a better appearance and help them see.

Keep reading for more on treating Fraser syndrome effectively.

Genetic Counseling

Since an autosomal recessive genetic disorder is the reason for Fraser syndrome, parents are recommended to seek genetic counseling. This type of counseling provides advice to prospective parents concerned about their children being born with Fraser syndrome or other genetic conditions. The gene is passed onto to the child by a combination of chromosomes from both the mother and father. This may cause concern for expecting parents who carry this genetic disorder. Chromosomes are present in the cells of human beings and contain the genetic information for everyone. The cells in the human body have forty-six chromosomes that contain the genetics passed down to children from their parents.

Fraser syndrome is carried in the chromosomes with abnormal genes. When parents participate in genetic counseling, a counselor will aid them in understanding how genetics may affect their unborn child. They can also explain how the family can cope with life if they have a child with this disorder. A genetic counselor evaluates the family's medical history and provides information about the baby’s risk of developing a medical disorder. The counselor will also arrange genetic tests for and assist with making healthcare plans.

Get to know the next option for treatment now.