Gerstmann-Straussler-Scheinker syndrome

Gerstmann-Straussler-Scheinker syndrome (GSSS) is a particular and rare form of human transmissible spongiform encephalopathy (TSE) due to a defective gene encoding the prion protein (<i>PRNP</i> gene) and marked by particular multicentric amyloid plaques in the brain.

Optic atrophy

Atrophy of the optic nerve. Optic atrophy results from the death of the retinal ganglion cell axons that comprise the optic nerve and manifesting as a pale optic nerve on fundoscopy.


Total: 2

                      


(per page)
PMID (PMCID)
11257791
MALE Middle Aged
[A case of Gerstmann-Straussler-Scheinker syndrome (P102L) accompanied by optic atrophy].
Sugai F, Nakamori M, Nakatsuji Y, Abe K, Sakoda S.
Rinsho Shinkeigaku. 2000;40(9):926-8.
We report a patient with Gerstmann-Straussler-Scheinker syndrome (GSS102) who developed optic atrophy.
11257791
MALE Middle Aged
[A case of Gerstmann-Straussler-Scheinker syndrome (P102L) accompanied by optic atrophy].
Sugai F, Nakamori M, Nakatsuji Y, Abe K, Sakoda S.
Rinsho Shinkeigaku. 2000;40(9):926-8.
[A case of Gerstmann-Straussler-Scheinker syndrome (P102L) accompanied by optic atrophy].