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Tuberous sclerosis
? TBD
Genetic condition causing non-cancerous tumours
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tuberous sclerosis 1
Tuberous sclerosis mapped to chromosome 9q34 (TSC1 gene)
Subject of
5
Fetal and maternal manifestations of tuberous sclerosis complex: Value of fetal MRI.
scientific article published on 02 February 2016
The effect of mTOR inhibition on obstructive hydrocephalus in patients with tuberous sclerosis complex (TSC) related subependymal giant cell astrocytoma (SEGA)
scientific article published on 13 April 2020
Extrapulmonary uterine lymphangioleiomyomatosis (LAM) and dysfunctional uterine bleeding: the first presentation of LAM in a tuberous sclerosis complex patient
Brain lesions in tuberous sclerosis complex. Review.
scientific article published on January 2010
Regionally specific TSC1 and TSC2 gene expression in tuberous sclerosis complex
scientific article published in Scientific Reports
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Tuberous sclerosis complex (TSC) is a rare multisystem autosomal dominant genetic disease that causes non-cancerous tumours to grow in the brain and on other vital organs such as the kidneys, heart, liver, eyes, lungs and skin. A combination of symptoms may include seizures, intellectual disability, developmental delay, behavioral problems, skin...

Instance of
designated intractable/rare disease
Rare disease
class of disease
Subclass of
autosomal dominant disease
Syndrome
Disease
Different from
Tuberculosis
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