Thrombotic thrombocytopenic purpura classification: Difference between revisions
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==Overview== | ==Overview== | ||
== Classification == | == Classification == | ||
* '''Hereditary:''' Insertions, deletions, missense, nonsense point mutations and splice site mutations of both alleles of ADAMS13 genes cause decrease in the amount and activity of the enzyme. | * '''Hereditary:''' congenital TTP, inherited TTP, familial TTP, Upshaw-Schulman syndrome (USS) is an autosomal recessive diseas | ||
Insertions, deletions, missense, nonsense point mutations and splice site mutations of both alleles of ADAMS13 genes cause decrease in the amount and activity of the enzyme. | |||
* '''Acquired:''' Existence of an inhibitory antibody against ADAMS13 due to variety of conditions. | * '''Acquired:''' Existence of an inhibitory antibody against ADAMS13 due to the variety of conditions. | ||
==References== | ==References== | ||
Revision as of 17:14, 7 August 2018
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Thrombotic thrombocytopenic purpura Microchapters |
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Differentiating Thrombotic thrombocytopenic purpura from other Diseases |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Saeedeh Kowsarnia M.D.[2]
Overview
Classification
- Hereditary: congenital TTP, inherited TTP, familial TTP, Upshaw-Schulman syndrome (USS) is an autosomal recessive diseas
Insertions, deletions, missense, nonsense point mutations and splice site mutations of both alleles of ADAMS13 genes cause decrease in the amount and activity of the enzyme.
- Acquired: Existence of an inhibitory antibody against ADAMS13 due to the variety of conditions.