TITLE: Gauchers Disease]

OBJECTIVES:
1. To be able to understand Gauchers Disease.
2. To be able to know the cause of Gaucher’s Disease.
3. To able to know the different sign and symptoms of Gaucher’s Disease.

INTRODUCTION:

Gauchers Disease - is inherited metabolic disorders in with harmful quantities of a fatty substance culled glucocerebroside accumulate in the spleen, liver, lungs bone marrow and sometimes in the brain.

Gauehers Disease was an inherited disease and that both parents must pass on the gene for the disease. It involves also the Sphingolipidoses a lysosomal hydrolytic enzyme is difficult in each disorder. The enzyme is difficult in each disorder. The enzyme deficiencies cause death usually soon after the first month of life with the exception of the adult form of Gauehers disease and of Fabrys disease. The sphinyotipidoses are autosomal recessive disease.

ETIOLOGY

What is Gauchers Disease?

Gauchers disease is an inherited metabolic......

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Title: Gauchers Disease
Approximate Word Count: 1607
Approximate Pages: 7 (250 words per double-spaced page)

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