📂 Diseases
primary congenital glaucoma 3A — Definition
primer konjenital glokom 3A / primary congenital glaucoma 3A
Primary congenitalital 3A is a genetic eye disease, characterized by abnormal height of intraocular pressure in birth or early childhood. This condition occurs as a result of developmental anomalies of drainage channels (trabecular network) in the front of the eye and can lead to optical nerve damage. Symptoms include watering in eyes, sensitivity to light, corneal blur and growth in the eyeball (buftalmi). Early diagnosis and surgical intervention have critical importance to prevent loss of vision.
Frequently Asked Questions
❓ What is primer konjenital glokom 3A?
primer konjenital glokom 3A; primary congenitalital 3A is a genetic eye disease, characterized by abnormal height of intraocular pressure in birth or early childhood. This condition occurs as a result of developmental anomalies of drainage channels (trabecular network) in the front of the eye and can lead to optical nerve damage. Symptoms include watering in eyes, sensitivity to light, corneal blur and growth in the eyeball (buftalmi). Early diagnosis and surgical intervention have critical importance to prevent loss of vision.
❓ What is primary congenital glaucoma 3A in Turkish?
The Turkish equivalent of "primary congenital glaucoma 3A" is primer konjenital glokom 3A.
❓ Which medical field is primer konjenital glokom 3A related to?
This term belongs to the Diseases category.