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Regd.no. - 0701216154
Branch- IT
SEMESTER- 7th
ACKNOWLEDGEMENT
Rod cells pick up movement out of the corner of the eye and
also, in a normal eye it is the rods that operate in poor light or at
night. There are about 120 million rods in each eye and they are
more numerous towards the outer edge of the retina
The cone cells are used in colour vision and in close precision
work like reading. There are not as many cones and they are
more concentrated in the centre of the retina (the Macula).
Disease of eye
• Retinitis pigmentosa
• Macular degeneration
Retinitis pigmentosa
Retinitis Pigmentosa (RP) is the name given to a group of
hereditary diseases of the retina of the eye. RP may be caused by
a breakdown in the function of the rods or the cones in some
part of the retina. The retina is so complex that breakdowns may
occur in a variety of ways and so RP is not a single disorder but
a great number of disorders. The breakdown of cone function
may be called Macular Degeneration.
Macular Degeneration
Macular is a sensitive area in the centre of the retina which
provides us with sight in the centre of our field of vision. It
allows us to see the fine details when we look directly at
something. In macular degeneration, a layer beneath the retina,
called the retinal pigment epithelium (RPE), gradually wears out
from its lifelong duties of disposing of retinal waste products.
A large proportion of macular degeneration cases
are age- related. Age related Macular Degeneration (AMD)
usually affects people over the age of 50 and there are two
distinct types - "wet" AMD and "dry" AMD. "Wet" AMD
results from the growth of new blood vessels in the choroid,
causing an accumulation of fluid in the macula which leads to
retinal damage. This type of degeneration can often be
successfully arrested by laser surgery.
"Dry" AMD represents at least 80% of all AMD cases and
results in atrophy of the Retina. Usually yellowish-white round
spots called drusen first appear in a scattered pattern deep in the
macula. Later degeneration of both the Pigment Epithelium and
the cones begins. While AMD is not inherited in a predictable
way, heredity may be involved to some extent.
BIONIC EYE
Advantages
Although the device will not be able to restore the eye sight of
the entire blind community, researchers are certain many
people will benefit from the technology. For instance, age-
related macular generation is the leading cause of blindness in
the industrialized world, with about 2 million Americans
currently suffering from the condition. The new technology will
hopefully assist people suffering from this condition, and
individuals suffering from retinitis pigmentosa (a genetic
condition), but will not help glaucoma patients.
Disadvantages
The scientists explain that the bionic eye will be affective for
individuals who once had sight, since their brain knows how to
process visual information. The unfortunate people who were
born blind do not have the neurological capability to process
the data received via the wire. Furthermore, the optic nerve
must be at least partly functional. Otherwise, the data will not
be fully processed. For many individuals that were born blind,
this is a problem as well, since their optic nerve has never been
used. This new technology will not be helpfull for glaucoma
patients.
CONCLUSION
Its been 6 years since Amme Larson received the first fully
implanted bionic eye at Karolinska Institute in Stockholm.
Researchers throughout the world have looked the way to
improve people’s lives with bionic devices.
Bionic devices are being developed to do more than
replace defective parts.
Providing power to run bionic implants and making
connection to the brain control system pose the two great
challenges for biomedical engineering.
Researchers are now looking at devices like bionic arms,
tongues and nose.