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Tuberous sclerosis

Authoring team

Tuberous sclerosis is a congenital disease characterised by hamartomatous lesions in the skin, nervous system and internal organs, principally heart and kidney.

It is dominantly inherited but many cases result from new mutations.

The most frequent presentation is a triad of:

  • adenoma sebaceum:
    • actually an angiofibroma with passive involvement of sebaceous glands
  • epilepsy
  • mental retardation

Click here for example images of this condition

Reference

  1. Wang M et al. Tuberous Sclerosis: Current Update. Radiographics. 2021 Nov-Dec;41(7):1992-2010

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The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

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