Neurology · Neurology / Neurocutaneous disorders
Tuberous sclerosis complex
also: Bourneville disease
Autosomal dominant hamartoma syndrome.
- Specialty
- Neurology
- Subspecialty
- Neurology / Neurocutaneous disorders
- Sex & age distribution
- Male: affected; Female: affected equally; Children: yes, infancy
- Gene(s) involved
- TSC1, TSC2
- Alternative names & eponyms
- Bourneville disease
Etiology & mechanism
TSC1 or TSC2 mutation.
Gene(s) involved (2)
Symptoms & signs (5)
In plain terms, someone with Tuberous sclerosis complex may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
Drag nodes, scroll to zoom, click a node to open that syndrome.
Shares symptoms with
1 shared
Action myoclonus–renal failure syndrome
seizures
1 shared
Aicardi syndrome
infantile spasms
1 shared
Alcohol withdrawal syndrome
seizures
1 shared
Amniotic fluid embolism syndrome
seizures
1 shared
Angelman syndrome
seizures
1 shared
Barakat syndrome
seizures
1 shared
Behçet syndrome
skin lesions
1 shared
Borjeson–Forssman–Lehmann syndrome
seizures
1 shared
Cardiofaciocutaneous syndrome
seizures
1 shared
Cerebral folate deficiency syndrome
seizures
Shares genes with
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