| Literature DB >> 22068806 |
Allysson Antonio Ribeiro Gomes1, Ylka Virginia Ribeiro Gomes, Felipe Barbosa Lima, Salustiano Gomes de Pinho Pessoa.
Abstract
Tuberous sclerosis is a rare genetic disease with autosomal dominant inheritance, associated with multiple hamartomas in several organs, such as the brain, skin, lung, kidney, heart and eyes. The authors of this study report a case of a 30 years old female patient with tuberous sclerosis, presenting multiple angiofibromas on face treated with high frequency equipment (radiofrequency), and discuss the therapeutic options for treatment of individuals with extensive cutaneous involvement in tuberous sclerosis.Entities:
Mesh:
Year: 2011 PMID: 22068806 DOI: 10.1590/s0365-05962011000700048
Source DB: PubMed Journal: An Bras Dermatol ISSN: 0365-0596 Impact factor: 1.896