Purtscher retinopathy as an initial presentation of thrombotic thrombocytopenic purpura
β Scribed by I. Tajunisah; D. K. Patel; V. Subrayan
- Publisher
- Springer US
- Year
- 2009
- Tongue
- English
- Weight
- 183 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0929-5305
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π SIMILAR VOLUMES
Thrombotic thrombocytopenic purpura (TTP) is a syndrome of unknown aetiology in which disseminated platelet thrombi are formed in capillaries and small arterioles throughout the entire body'\*2. Every organ can be involved in this diffuse process, but the relative frequency is different. T h e class
Thrombotic thrombocytopenic purpura (TTP) is an uncommon but severe disorder that classically presents with microangiopathic hemolytic anemia (MAHA), thrombocytopenia, and fluctuating neurological changes. Previously, it was impossible to make a diagnosis of TTP in the absence of thrombocytopenia or