The Tuberous Sclerosis Complex
University of Pennsylvania · Fox Chase Cancer Center
Indexed incrossrefpubmed
Abstract
The tuberous sclerosis complex (TSC), a multisystem, autosomal dominant disorder affecting children and adults, results from mutations in one of two genes, TSC1 (encoding hamartin) or TSC2 (encoding tuberin). In this article, the current knowledge of the pathogenesis of the disease and its management are discussed.
Citation impact
1,774
total citations
- FWCI
- 35.00
- Percentile
- 100%
- References
- 98
Citations per year
Authors
3Topics & keywords
Topics
Keywords
- Tuberous sclerosis
- TSC2
- TSC1
- Medicine
- Pathogenesis
- Disease
- Gene
- Genetics
UN Sustainable Development Goals
- Good health and well-being
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