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Polycystic Kidney Disease

Published on Nov 18, 2015

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PRESENTATION OUTLINE

POLYCYSTIC KIDNEY DISEASE

DANI GIL DE LEYVA

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)

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

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

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

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

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

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