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Lysosomal Storage Disease

Published on Nov 19, 2015

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PRESENTATION OUTLINE

NIEMANN- PICK DISEASE

MANASA MUPPIRALA, NATHAN GANTCHEV, JERRIN JACOB, CHIJIOKE UGWULEBO, BRIAN PAK
Photo by TheJCB

Organelle

THE ORGANELLE ASSOCIATED WITH THIS DISEASE IS THE LYSOSOME.

FUNCTION

BREAK DOWN MATERIALS IN THE CELL SUCH AS WASTE.

STRUCTURE

  • Lysosomes are enclosed by a single-layer membrane that allows the
  • remainder of the cell to be protected from the harsh digestive enzymes
  • that lysosomes use to break down and rid the cell of unwanted materials.
  • This membrane also allows the lysosome to maintain an acidic
  • environment similar to that of the stomach that aids in this same digestion.

DISEASE

  • If lysosomes are not breaking down the lipids, an excess amount will
  • build up and will have to find storage somewhere. This could possibly
  • explain for the enlarged liver and spleen found within Maudie's body.
  • This facilitation of poor lipid storage could clog blood vessels and cause
  • problems such as neural degeneration.