Neurology - tuberous sclerosis Flashcards
What is tuberous sclerosis?
A genetic condition that causes features in multiple systems
Characteristic feature is the development of many hamartomas in different parts of the body
What are hamartomas?
Benign neoplastic growths of the tissue that they originate from. Commonly affect:
- Skin
- Brain
- Lungs
- Heart
- Kidneys
- Eyes
They cause problems based on the tissue they occur in
What are the mutations seen in tuberous sclerosis?
Tuberous sclerosis is caused by mutations in one of two genes:
- TSC1 gene on chromosome 9, which codes for hamartin
- TSC2 gene on chromosome 16, which codes for tuberin
What do hamartin and tuberin do? What is the effect of mutation in the genes encoding these?
Hamartin and tuberin interact with each other to control the size and growth of cells.
Abnormalities in one of these proteins leads to abnormal cell size and growth.
Classical skin features seen in tuberous sclerosis
Ash leaf spots are depigmented areas of skin shaped like an ash leaf
Shagreen patches are thickened, dimpled, pigmented patches of skin
Angiofibromas are small skin coloured or pigmented papules that occur over the nose and cheeks
Subungual fibromata are fibromas growing from the nail bed. They are usually circular painless lumps that grow slowly and displace the nail
Cafe-au-lait spots are light brown “coffee and milk” coloured flat pigmented lesions on the skin
Poliosis is an isolated patch of white hair on the head, eyebrows, eyelashes or beard
What are the neurological features of tuberous sclerosis?
Epilepsy
Learning disability and developmental delay
Other features of tuberous sclerosis
Rhabdomyomas in the heart
Gliomas (tumours of the brain and spinal cord)
Polycystic kidneys
Lymphangioleiomyomatosis (abnormal growth in smooth muscle cells, often affecting the lungs) - multiple lung cysts
Retinal hamartomas
What is the classical presentation of someone with tuberous sclerosis?
A child presenting with epilepsy found to have skin features of tuberous sclerosis.
It can also present in adulthood.
Management of tuberous sclerosis
Management is supportive with monitoring and treating complications such as epilepsy.
There is no treatment for the underlying gene defect.