What is tuber scoliosis?
Overview. Tuberous sclerosis (TWO-bur-uhs skluh-ROH-sis), also called tuberous sclerosis complex, is an uncommon genetic disorder that causes noncancerous (benign) tumors — unexpected overgrowths of normal tissue — to develop in many parts of the body.
What causes ash leaf spots?
The typical skin manifestations of tuberous sclerosis are light patches due to decreased pigment. These are sometimes called ash leaf spots due because the shape resembles the leaf of an ash tree.
What are the signs of tuberous sclerosis complex?
Symptoms of tuberous sclerosis
- White spots on your skin that glow under a special lamp.
- A rash on your face that may look like acne.
- Problems with your kidneys.
- Areas of very thick skin, often on your back.
- Growths under or around your nails.
- Pitted teeth.
- Mental disabilities.
- Developmental delays.
Does tuberous sclerosis have a cure?
Unfortunately, there is no cure for tuberous sclerosis complex yet. But there are many effective treatment options for most symptoms. Antiepileptic medications can help treat and control infantile spasms and other types of seizures associated with TSC.
How to pronounce tuberous sclerosis?
In children and adults younger than 25 years,a magnetic resonance imaging (MRI) of the brain is performed every one to three years to monitor for subependymal giant cell astrocytoma
How does tuberous sclerosis affect the body?
– Skin abnormalities. Most people with tuberous sclerosis have patches of light-colored skin, or they may develop small, harmless areas of thickened, smooth skin or reddish bumps under or around the – Seizures. – Cognitive disabilities. – Behavioral problems. – Kidney problems. – Heart issues. – Lung problems. – Eye abnormalities.
What is the history of tuberous sclerosis?
Tuberous sclerosis results from alterations (mutations) in a gene or genes that may occur spontaneously (sporadically) for unknown reasons or be inherited as an autosomal dominant trait. Most cases represent new (sporadic or de novo) gene mutations, with no family history of the disease.