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"Irido-corneo-trabecular" dysgenesis
Did you mean "Irido-cornea-trabecular" dysgenesis?
- ... each cell is sufficient to cause the disorder. Irido-corneo-trabecular dysgenesis Peters congenital glaucoma Genetic Testing Registry: Anterior segment ...
- ... the FOXC1 gene have been found to cause Peters anomaly. This condition is characterized by abnormal development of ... clouding of the cornea. The mutations that cause Peters anomaly likely disrupt the protein's ability to regulate ...
- ... of the eye (cornea). An eye problem called Peters anomaly is the most common anterior segment abnormality seen in Peters plus syndrome. Peters anomaly involves abnormal development of the anterior segment, which ...
- ... the PAX6 gene have been found to cause Peters anomaly. This condition is characterized by the abnormal development ... of the eye (cornea). The mutations that cause Peters anomaly change single protein building blocks (amino acids) in ...
- ... the PITX2 gene has been found to cause Peters anomaly. This condition is characterized by abnormal development of ... area of the eye and other features of Peters anomaly. More About This Health Condition Mutations in the ...
- ... the CYP1B1 gene have been found to cause Peters anomaly. This condition is characterized by abnormal development of ... of the eye (cornea). The variants that cause Peters anomaly likely impair the normal function of the CYP1B1 ...
- Corneal Disorders (National Library of Medicine)Your cornea is the outermost layer of your eye. It is clear and shaped like a dome. The cornea helps to shield the rest of the eye from germs, dust, and other ...