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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 disorder in which harmful quantities of a fatly substance called glucocerebroside accumulate in the spleen, liver, lungs, bone marrow, and sometimes in the brain. There are three types of Gaudier disease...
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