100% satisfaction guarantee Immediately available after payment Both online and in PDF No strings attached 4.2 TrustPilot
logo-home
Summary

Summary Tears for diagnostic testing of brain disease

Rating
-
Sold
-
Pages
12
Uploaded on
25-11-2025
Written in
2025/2026

This lecture is given by Prof. Gijs in the Translational Neuroscience course. The summary is based on the given slides and my own notes.

Institution
Module











Whoops! We can’t load your doc right now. Try again or contact support.

Written for

Institution
Study
Module

Document information

Uploaded on
November 25, 2025
Number of pages
12
Written in
2025/2026
Type
Summary

Subjects

Content preview

Tears for diagnostic testing of brain disease
(Prof. Gijs)
1. Anatomy of the eye
 In front of the iris is the cornea
 Cornea is transparent because light needs to go through
 Anterior chamber is between the lens and cornea which is filled with fluid
 Posterior part of the eye  lined with retina
 In retina is a complete inner lining which contain neuron cells  travel to
optic disc  transmit visual signals into neural signals
o The retina is composed of 10 layers
o Rods and cones catch visual signals and transform them into
neuronal signals
 A lot of muscles surrounding the eye because you can move the eye in
different directions
 Blood vessels in the eye




2. Three most common eye diseases
2.1. Cataract
= disease of the lens  lens is refracting visual signals  with cataract you
have no sharpening of your vision

2.1.1.Definition and causes
 = clouding of the lens
 Slow progression and painless
 Pictures
o Left




1

,  Healthy individual: lens is refracting the eye to the center 
centering then you get a sharp vision
o Right = cataract
 Not centralized in the retina = blurry vision
 Causes
o Age
o Metabolic disease (eg diabetes)
o Ocular diseases (eg uveitis)
o Ocular surgery
o Trauma
o Congenital
o Medication (eg steroids)
 Treatment = lens which is replacing your original lens?

2.1.2.Symptoms
 Decreased vision
 Halo’s = light sources  very large glow around it
 Monocular diplopia = double vision in one eye




2.2. Glaucoma
= disease of the papil
 Progressive neuropathy
 (A) Excavation optic disc, thinning of nerve fibers
o All nerves and axons come together and go to the brain
o Healthy: small entry side with a lot of nerves and blood vesels
o Glaucoma has a larger entry side
 (B) Visual field loss
o They will still have a sharp image but in the periphery they will lose
vision
o Sharp central vision but not complete because loss of visual field
o They don’t see black spots because the brain is filling it in
A B




2

,  Neuroretinal rim
 Cup/disc ratio = diameter of cup expressed as fraction of diameter of disc
 Picture
o Blue: optic cup
o Green: optic disc
o Inbetween is a rim
 Rim is decreasing and cup is altered
o Upper donut is healthy example




 Visual field loss
 Very slowly progressive, brain fills in missing spots
o Damage is irreversible and difficult to treat  tunnel vision in late
stages




2.2.1.Glaucoma main risk factor = increase intraocular pressure (IOP)
 Misbalance between aqueous humor production and outflow
 Not directly the cause
 Normal IOP because the eye is a closed ball
o Pressure increases  press against tissues of the eye  especially
the retina
o Signals cannot travel to the brain
 IOP is caused by misbalance between production and outflow

3

, o Production is normal but outflow is blocked

2.2.2.Treatment
 Medication, topical eye drops
o Reduce aqueous humor production (eg beta blokkers)
o Increase aqueous humor outflow (eg prostaglandins)
 Laser: shoot wholes to increase drainage
 Surgery: fluid is given an alternative outflow
o Trabeculectomy (bleb)
o Implants (drainage)
o Shunts

2.3. Age-related macula degeneration (AMD)
= disease of the retina
= degeneration of the macula
 Types of AMD
o Dry AMD (90%)
 No exucative
 No neovascularisation
o Wet AMD (10%)
 Exucative
 Neovascularization
 Fast progression, fast loss of vision
 Observations in the retina
o Drusen = extracellular waste products between RPE and Bruch
membrane




o Hyper- and hypopigmentation on the RPE
o Atrophy RPE (degeneration)




2.3.1.AMD symptoms (dry AMD)
 Gradual vision loss over months/years
 (A) Metamorphopsia = deformation of the squares
 (B) (Para)central scotoma = black spot in the center of your vision
B




4
£5.40
Get access to the full document:

100% satisfaction guarantee
Immediately available after payment
Both online and in PDF
No strings attached

Get to know the seller
Seller avatar
WillemsenAmber
4.0
(1)

Also available in package deal

Get to know the seller

Seller avatar
WillemsenAmber Universiteit Antwerpen
Follow You need to be logged in order to follow users or courses
Sold
10
Member since
1 year
Number of followers
0
Documents
45
Last sold
1 week ago

4.0

1 reviews

5
0
4
1
3
0
2
0
1
0

Recently viewed by you

Why students choose Stuvia

Created by fellow students, verified by reviews

Quality you can trust: written by students who passed their exams and reviewed by others who've used these revision notes.

Didn't get what you expected? Choose another document

No problem! You can straightaway pick a different document that better suits what you're after.

Pay as you like, start learning straight away

No subscription, no commitments. Pay the way you're used to via credit card and download your PDF document instantly.

Student with book image

“Bought, downloaded, and smashed it. It really can be that simple.”

Alisha Student

Frequently asked questions