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Difference between revisions of "Gaucher disease"
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→Subtypes: mor
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m (→Subtypes: mor) |
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Types:<ref name=Ref_PCPBoD8_95>{{Ref PCPBoD8|95}}</ref> | Types:<ref name=Ref_PCPBoD8_95>{{Ref PCPBoD8|95}}</ref> | ||
*Type I: 99% of cases; no CNS | *Type I: 99% of cases; no CNS involvement - survive to adulthood. | ||
*Type II: infantile. | *Type II: infantile onset - CNS degeneration + death at young age. | ||
*Type III: mixed of type I & type II. | *Type III: mixed of type I & type II. | ||