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Neurofibromatosis

Published on Nov 22, 2015

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PRESENTATION OUTLINE

NEUROFIBROMATOSIS

BY:JARED JONES, DUNCAN BERGER, SARAH SINGLETON, AND ANANYA BASHYAM

YOUR CHILD'S SYMPTOMS

  • Cafe-au-lait spots
  • Optical glicomas,reduced vision
  • Learning disabilities
  • Unusually large head
  • Appearance of lisch nodules

MORE POSSIBLE SYMPTOMS

  • Multiple noncancerous tumors
  • High blood pressure
  • Scoliosis
  • Bone defects
  • Early puberty

TREATEMENT

  • There is no cure for NF1
  • However, there are treatment options
  • for each individual symptom
  • Not all symptoms may present
  • Visit a specialist on a scheduled basis

KEEP AHEAD OF NF1

  • Make yearly visits with an optometrist.
  • Have an orthopedist on standby in the earlier years.
  • Have regular visits with a chiropractor.
  • Have your child's blood pressure checked regularly.

INHERITANCE

  • NF1 is an autosomal dominant disease
  • This means that it is passed genetically
  • NF1 requires two genes to be mutated to form tumors