Madcow and Mad "Human" Disease

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Mad Cow and Mad Human

Diseases

By: Alif Rizal Efendi (14210068)

Bovine spongiform encephalopathy (BSE), commonly


known as mad cow disease, is a fatal neurodegenerative
disease in cattle that causes a spongy degeneration in
the brain and spinal cord. BSE has a long incubation
period, about 30 months to 8 years, usually affecting
adult cattle at a peak age onset of four to five years,
all breeds being equally susceptible. In the United
Kingdom, the country worst affected, more than
180,000 cattle have been infected and
4.4 million slaughtered during the eradication program.

CreutzfeldtJakob disease or CJD is


a degenerative neurological disorder (brain disease)
that is incurable and invariably fatal. CJD is at times
called a human form of mad cow disease even though
classic CJD is not related to bovine spongiform
encephalopathy, however, given that bovin spongiform
encephalopathy is believed to be the cause of variant
CreutzfeldtJakob (vCJD) disease in humans, the two
are often confused.[4]
Variant CJD (vCJD) is the most common among the types
of transmissible spongiform encephalopathy found in
humans. In CJD, the brain tissue develops holes and
takes on a sponge-like texture. This is due to a type of
infectious protein called a prion.

Signs and symptomps :


The first symptom of CJD is rapidly progressive dementia,
leading to memory loss, personality changes
and hallucinations. This is accompanied by physical
problems such as speech impairment, jerky movements
(myoclonus), balance and coordination dysfunction
(ataxia), changes in gait, rigid posture, and seizures.

Necessary Information :
A prion is an infectious agent composed of protein in
a misfolded form. This is in contrast to all other known
infectious agents (virus/bacteria/fungus/parasite)
which must contain nucleic acids (either DNA, RNA, or
both). The word prion, coined in 1982 by Stanley B.
Prusiner, is derived from the
words protein and infection.[3] Prions are responsible for
the transmissible spongiform encephalopathies in a
variety of mammals, including bovine spongiform
encephalopathy (BSE, also known as "mad cow
disease") in cattle and CreutzfeldtJakob disease (CJD)
in humans. All known prion diseases affect the structure
of the brain or other neural tissue and all are currently
untreatable and universally fatal.

Dementia (taken from Latin, originally meaning "madness",


from de- "without" + ment, the root of mens "mind") is a
serious loss of global cognitiveability in a previously
unimpaired person, beyond what might be expected
from normal aging. It may be static, the result of a
unique global brain injury, or progressive, resulting in
long-term decline due to damage or disease in the body.

Sources :
http://en.wikipedia.org/wiki/Mad_cow
http://en.wikipedia.org/wiki/Creutzfeldt%E2%80%93Jako
b_disease
http://en.wikipedia.org/wiki/Prion
http://en.wikipedia.org/wiki/Dementia

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