Tuberous Sclerosis: A Case Report and Review of the Literature

Tuberous sclerosis (TS) is a rare genetic disorder of autosomal-dominant inheritance. Mutations on either of the two genes Tuberous Sclerosis Complex 1 (TSC1) or Tuberous Sclerosis Complex 2 (TSC2) play a role and result in hamartomas involving many organs, like the brain, heart, kidneys, skin, lung...

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Detalles Bibliográficos
Autores principales: Dzefi-Tettey, Klenam, Edzie, Emmanuel K, Gorleku, Philip, Piersson, Albert D, Cudjoe, Obed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Dermatology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854338/
https://www.ncbi.nlm.nih.gov/pubmed/33552794
http://dx.doi.org/10.7759/cureus.12481

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854338/
https://www.ncbi.nlm.nih.gov/pubmed/33552794
http://dx.doi.org/10.7759/cureus.12481

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