Purpura fulminans as a sequel to erythema nodosum in a child with homozygous Leiden mutation and acquired protein S deficiency. [electronic resource]
Producer: 20060106Description: 1155-8 p. digitalISSN:- 0803-5253
- Biopsy, Needle
- Child
- Combined Modality Therapy
- Erythema Nodosum -- complications
- Factor V -- genetics
- Follow-Up Studies
- Heparin -- therapeutic use
- Humans
- IgA Vasculitis -- complications
- Immunohistochemistry
- Male
- Plasma Exchange
- Point Mutation
- Prednisolone -- therapeutic use
- Protein S Deficiency -- complications
- Risk Assessment
- Severity of Illness Index
- Treatment Outcome
- Warfarin -- therapeutic use
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Publication Type: Case Reports; Journal Article
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