Tuberous Sclerosis 2 C1860707
A genetic condition causing non-cancerous tumors in multiple organs. Often involves the brain, skin, and kidneys. Regular monitoring and symptom management are key.
Key facts at a glance
- ICD-10
- G40.909
- ICD-11
- 8A00.0
- Body system
- neurologic
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Warning signs - seek immediate care
Severe headache
Generalized symptoms
(neurologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Infantile spasms
(neurologic)Cortical dysplasia
(neurologic)Subependymal giant cell astrocytoma
(neurologic)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Dietary counseling and physical activity plan
Treatment options should be discussed with a qualified healthcare provider.
mTOR Inhibitor Therapy
Everolimus or sirolimus therapy for TSC2 to inhibit abnormal cell growth, reduce subependymal giant cell astrocytoma size, treat renal angiomyolipomas, and manage skin lesions.
Everolimus for Refractory Seizures
Adjunctive everolimus specifically for treatment-resistant seizures in TSC2, which may reduce seizure frequency significantly in many patients.
Additional treatment options
Surgical Intervention for SEGA
Neurosurgical procedures for subependymal giant cell astrocytomas causing obstructive hydrocephalus, significant mass effect, or refractory symptoms despite medical therapy.
procedureRenal Intervention for Angiomyolipomas
Embolization, nephron-sparing surgery, or ablation techniques for bleeding or large angiomyolipomas, preserving kidney function while preventing complications.
procedureTSC Center of Excellence Follow-up
Regular multidisciplinary follow-up at a TSC clinic or center of excellence coordinating neurology, nephrology, dermatology, genetics, and developmental services.
monitoringWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Tuberous Sclerosis 2 C1860707?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Northrup H, et al. Updated International Tuberous Sclerosis Complex Consensus Group Clinical Diagnostic Criteria for Tuberous Sclerosis Complex. Pediatric Neurology. 2021;124:1-10.
Franz DN, et al. Efficacy and safety of mTOR inhibitors in tuberous sclerosis complex: A randomized controlled trial. Lancet Neurology. 2019;18(11):1016-1025.
Kingswood JC, et al. The association between renal angiomyolipomas and lymphangioleiomyomatosis in tuberous sclerosis complex: A meta-analysis. Kidney Int. 2016;90(4):784-790.
Curatolo P, et al. Mechanistic target of rapamycin pathway in tuberous sclerosis complex: A comprehensive review. Lancet Neurology. 2020;19(8):654-669.
Medication Comparisons
Compare medications used to treat Tuberous Sclerosis 2 C1860707. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy