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Polycystic Kidney Disease
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Published on Nov 18, 2015
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PRESENTATION OUTLINE
1.
POLYCYSTIC KIDNEY DISEASE
DANI GIL DE LEYVA
2.
WHO DISCOVERED IT?
Polycystic kidney disease was discovered by Richard Bright
He was a British researcher and physician
There are 2 types of polycystic kidney disease
autosomal dominant PKD (50% chance)
autosomal recessive PKD (rare)
3.
CURRENT STATUS
600,000 people have PKD in the U.S.
that a new drug (tolvaptan) can dramatically slow
The development of polycystic kidney disease
4.
SIGNS AND SYMPTOMS
blood in urine, continuous kidney infections
Kidney stones, pain in lower back, bad breath
Headaches, vomit, chest pains, itching skin
swelling of ankles and eyes, frequent urination
5.
WHAT SYSTEMS ARE AFFECTED
PKD affects the excretory system
PKD can occur when muscles and arteries expand
Children who have PKD could have hypertension
If you have PKD you can have really high blood pressure
6.
HOW DO YOU RECEIVE IT
PKD is passed down through families.
It has to be inherited
It is not sex linked because it is autosomal
It's a mutation but only for recessive PKD
7.
TREATMEMT
Some treatments are that a family can donate a kidneys To replace theirs
You can take medical treatments that will help reduced the damage of the kidneys
Other than that there is no real treatments that are available
8.
HOW IS IT DIAGNOSED
its diagnosed if both of the parent inherited
If it's dominant you start developing it from ages 30 & 40
Recessive- begins when you are new born or even in the womb.
When newborn you have enlarged kidneys with a weird appearance
9.
BIBLIOGRAPHY
http://www.kidney.org/atoz/content/polycystic.cfm
http://en.wikipedia.org/wiki/Polycystic_kidney_disease
http://kidney.niddk.nih.gov/kudiseases/pubs/polycystic/
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