Acute Hemolytic Anemia as an Initial Presentation of Wilson’s Disease
Amerah Mohamed Ahmed ElShahawy;
Abstract
Abstract
Wilson's disease (WD) is an autosomal recessive inherited disorder of copper metabolism resulting in pathological accumulation of copper in many organs and tissues. Hemolytic anemia (HA) in WD occurs in up to 17% of patients at some point i
Wilson's disease (WD) is an autosomal recessive inherited disorder of copper metabolism resulting in pathological accumulation of copper in many organs and tissues. Hemolytic anemia (HA) in WD occurs in up to 17% of patients at some point i
Other data
| Title | Acute Hemolytic Anemia as an Initial Presentation of Wilson’s Disease | Other Titles | أنيميا إنحلال الدم الحادة كعرض أولِى لمرض ويلسون | Authors | Amerah Mohamed Ahmed ElShahawy | Keywords | Acute Hemolytic Anemia as an Initial Presentation of Wilson’s Disease | Issue Date | 2012 | Description | Abstract Wilson's disease (WD) is an autosomal recessive inherited disorder of copper metabolism resulting in pathological accumulation of copper in many organs and tissues. Hemolytic anemia (HA) in WD occurs in up to 17% of patients at some point i |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 00_Amerah_THESIS_Final.pdf | 266.87 kB | Adobe PDF | View/Open |
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