
What is keratoconus?


3. irregular astigmatism
4. progressive disease
Risk factor?
1. pigmented skin/ dark skin
2. those live at high landed
3. 20-30 years old
4. frequent rubbing eye
5. genetic
6. contact lens
Onset?
around puberty
How to detect keratoconus?
This is for early detection.
1.retinoscopy--scissor movement (Scissor movement also will be seen in SPK)
2.ofthalmoscopy--oil droplet reflex
3.frequent changes of glasses
>other methods to detect keratoconus.
4.keratometry--high K-reading(normal k-reading:40-48D),mire cannot superimpose
5.pachymetry--thin cornea(normal corneal thickness=500-550nm)
However, there are variation between different people. Some people may have thin cornea and high K-reading naturally. Some are having low K-reading and thick cornea although they have keratoconus.
only seen in moderate to severe level.




Next time i will show you how to analyze the corneal topograph of keratoconus.
Management?
1.soft contact lens--Prefect K
2.RGP--Rose K, Igel K, Soflex

3.intact

CCL is to strengthen the corneal structure to reduce the progression of keratoconus. The vision after CCL will not improve so much, just 1-2 lines.

Corneal graft always the last option to treat the keratoconus. there are some risks of corneal graft like rejection and may induce glaucome(due to the steroid eyedrop after surgery).