
๐Overview
This condition arises from mutations in the TSC1 or TSC2 genes, which play a critical role in regulating cell growth and proliferation. These genetic changes lead to the uncontrolled growth of cells, resulting in hamartomas throughout the body. Common manifestations include skin lesions, seizures, and cognitive impairment. Management typically involves monitoring tumor growth and treating specific symptoms as they arise.
๐ก๏ธ Educational information only
This content is provided for general health education and awareness and is based on publicly available medical information. It is not intended to replace professional medical advice, diagnosis, or treatment, and should not be used to make healthcare decisions. Always seek the guidance of a qualified healthcare professional regarding any medical condition, medication, supplement, or procedure.
Additional Resources
Medical codes (for reference)
UMLS CUI: C0041341Codes are provided for reference and interoperability. They are not a diagnosis.
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