No cure; management focuses on addressing symptoms and improving quality of life; outcomes are variable, and the disease tends to progress over time
Gerstmann-Straussler-Scheinker disease (GSS) is a rare genetic disorder that leads to progressive neurological decline. There is no cure, and treatment focuses on managing symptoms and providing supportive care.
Rare, inherited prion disease that affects the nervous system
Progressive neurological symptoms, including ataxia (loss of coordination), cognitive decline, muscle stiffness
Genetic testing, imaging studies
Variable; progressive and fatal
Neurological deficits, complications of untreated GSS
Mutations in the PRNP gene, leading to the formation of abnormal prion proteins
Supportive care, symptom management; no specific treatment to alter the course of the disease
Supportive care, symptom management; no specific treatment to alter the course of the disease
Rare prion disease affecting the central nervous system
Supportive care focuses on managing symptoms and improving quality of life
For personalized advice and care, always seek the assistance of healthcare professionals. This information is meant for general understanding and not as a replacement for professional medical advice.
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