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Tuberous sclerosis Health Article
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Definition
Tuberous sclerosis is a group of two genetic disorders that affect the skin, brain/nervous system, kidneys, and heart, and cause tumors to grow. The diseases are named after a tuber- or root-shaped growth in the brain.
Alternative Names
Adenoma sebaceum
Causes, incidence, and risk factors
Tuberous sclerosis is inherited. Changes (mutations) in two genes, TSC1 and TSC2, are responsible for the condition. Only one parent needs to pass on the mutation for the child to get the disease. However, most cases are due to new mutations, so there usually is no family history of tuberous sclerosis. This condition is one of a group of diseases called neuro-cutaneous syndromes. Both the skin and central nervous system (brain and spinal cord) are involved. There are no known risk factors, other than having a parent with tuberous sclerosis. In that case, each child has a 50% chance of inheriting the disease.
Symptoms
Skin symptoms include:
Brain symptoms include: Other symptoms:
The symptoms of tuberous sclerosis vary from person to person. Some people have normal intelligence and no seizures. Others have severe retardation, serious tumors, or difficult-to-control seizures.
Signs and tests
Signs may include:
Tests may include: DNA testing for either of the two genes that can cause this disease (TSC1 or TSC2) is available. Regular ultrasound checks of the kidneys are an important screening tool, to make sure there is no tumor growth. |
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