CASE REPORT: An inherited APC mutation in the first reported Australian case of Turcot's syndrome
β Scribed by CONSTANTINE TOMARAS; DOROTHY M PAINTER; NUR J BASHA; DAVID J KOOREY
- Book ID
- 108949610
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 633 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0815-9319
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
A case of Turcot's syndrome is described in an 8-yearold girl. Turcot's syndrome is a rare hereditary disease in which malignant glioma of the central nervous system is associated with colonic polyposis. The patient initially presented with a left parietal glioblastoma diagnosed by computed tomograp
The association between hepatitis C virus (HCV) infection, cryoglobulinemia and urticarial vasculitis is well documented. However, urticarial vasculitis is extremely rare in HCV infection when not complicated by cryoglobulinemia. Here we describe a patient with urticarial vasculitis who had previous