What does TSC mean in PHYSIOLOGY
Tuberous Sclerosis Complex (TSC) is a rare genetic disorder that causes the growth of non-cancerous tumors in different parts of the body. It affects multiple organs, including the brain, eyes, heart, kidneys, skin, and lungs. People with TSC may experience seizures and intellectual disability as well as other neurological problems. It's estimated that approximately one in every 6,000 people have this condition worldwide.
TSC meaning in Physiology in Medical
TSC mostly used in an acronym Physiology in Category Medical that means Tuberous Sclerosis Complex
Shorthand: TSC,
Full Form: Tuberous Sclerosis Complex
For more information of "Tuberous Sclerosis Complex", see the section below.
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TSC Meaning
Tuberous Sclerosis Complex is an autosomal dominant genetic disorder caused by mutations in either of two genes. The first gene is TSC1 which is located on chromosome 9, and the second gene is TSC2 which is located on chromosome 16. These mutations lead to abnormal cell growth in multiple organs such as the brain, heart, skin and kidneys.
Symptoms
Symptoms of TSC vary depending on what part or parts of the body are affected by tumor growth. Common signs include seizures, developmental delay and intellectual disability as well as skin lesions such as white patches or red bumps on the face and scalp. Other signs and symptoms include kidney cysts or tumors on other organs such as the heart and lungs.
Diagnosis
Diagnosis typically begins with a physical examination followed by testing to determine if a person has changes in either TSC1 or TSC2 genes. If changes are found then imaging tests might be ordered to help determine where any tumors are located in the body.
Treatment
Treatment for TSC begins with managing any existing symptoms. Anti-seizure medications may be prescribed while hormone therapy can be used to help reduce tumor size. Surgery may also be indicated if tumors are causing problems in certain areas of the body such as obstructing normal flow of fluids from one organ to another.
Essential Questions and Answers on Tuberous Sclerosis Complex in "MEDICAL»PHYSIOLOGY"
What is Tuberous Sclerosis Complex (TSC)?
Tuberous Sclerosis Complex (TSC) is a rare genetic disorder that causes the growth of benign tumors in various organs, such as the heart, eyes, brain, skin and lungs. TSC can cause a variety of health problems including seizures, developmental delays, intellectual disabilities and behavioral problems. People with TSC have an increased risk of autism spectrum disorder (ASD) and kidney disease. Treatment typically involves medication to control seizures and other symptoms, and some people may require surgery to remove certain tumors if they are causing life-threatening complications.
How is Tuberous Sclerosis Complex diagnosed?
Diagnosis of Tuberous Sclerosis Complex (TSC) typically begins with a physical exam or imaging tests to identify any possible tumors that may be related to TSC. Genetic testing may also help confirm the diagnosis. A doctor will ask about your family history and any symptoms you might have experienced in order to make an accurate diagnosis. Depending on the symptoms present, additional medical tests such as blood tests or EEGs may be needed for confirmation.
What are the signs and symptoms of Tuberous Sclerosis Complex?
The signs and symptoms associated with Tuberous Sclerosis Complex (TSC) can vary widely from person to person depending on which organs are affected by tumor growth. Common signs and symptoms include epilepsy or seizures; intellectual disability; developmental delay; autism spectrum disorder; white patches on the skin due to abnormal bone deposition; benign tumors on the heart, lungs or kidneys; hypopigmented skin lesions; unusual behaviors; facial abnormalities such as an elongated face or mandibular prognathism (jaw overgrowth); vision impairments such as cataracts; hearing loss or deafness; enlarged lymph nodes; inadequate production of certain hormones from the pituitary gland; and excessive hair growth in certain areas of the body.
What causes Tuberous Sclerosis Complex?
Tuberous Sclerosis Complex (TSC) is caused by a genetic mutation in either one of two genes known as hamartin (TSC1) or tuberin (TSC2). These genes help regulate cell growth during development so when mutations occur they can lead to excessive cell growth which forms benign tumors throughout various organs in the body. The exact cause of these gene mutations remains unknown but it likely occurs randomly without reason or warning in most cases.
Is there a cure for Tuberous Sclerosis Complex?
Unfortunately there is no known cure for Tuberous Sclerosis Complex (TSC). However treatment options are available that can help manage many of its associated symptoms such as epileptic seizures, developmental delays, hormone deficiencies and other complications resulting from tumor growth within various organs across the body. These treatments are aimed at reducing symptom severity rather than curing it outright.
How can I find support if I am living with Tuberous Sclerosis Complex?
If you have been diagnosed with Tuberous Sclerosis Complex (TSC), seeking out support from others who understand what you’re going through can be incredibly beneficial for your mental health. There are numerous organizations focused specifically on helping those living with TSC so look for ones near you or join online support groups for information sharing and discussion among peers who understand your experience.
Does everyone with a mutation in their TSC1 gene necessarily develop features that meet clinical criteria for being classified as having tuberous sclerosis complex?
Not all people born with a mutation in their TSC1 gene will develop features that would qualify them clinically as having tuberous sclerosis complex according to current guidelines set out by medical professionals – however some people do go on to develop these features later on in their lives regardless.
Are there any risks associated with inherited forms of tuberous sclerosis complex?
Yes - while inherited forms of tuberous sclerosis complex generally have similar characteristics - they can still carry unique risks depending on where exactly their mutation lies within either gene involved i.e., TSC1 or TSC2 - meaning some cases may be more serious than others depending upon individual circumstances.
Are there any lifestyle changes that can help people cope better day-to-day with tuberous sclerosis complex?
Yes – it’s important for those living with tuberous sclerosis complex to adopt healthy lifestyle habits including getting plenty rest when possible, establishing regular meal times throughout each dayand exercising regularly when feeling able so as to stay active both physically & psychologically plus get into a consistent daily routine where possible too
Final Words:
Tuberous Sclerosis Complex is a rare but serious genetic disorder that can cause various problems throughout different parts of the body depending on where tumors grow. Early diagnosis and treatment can help manage symptoms and prevent further complications from occurring.
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