SciELO - Scientific Electronic Library Online

 
vol.86 issue1Case for diagnosisDo you know this syndrome? author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Article

Indicators

Related links

  • On index processCited by Google
  • Have no similar articlesSimilars in SciELO
  • On index processSimilars in Google

Share


Anais Brasileiros de Dermatologia

Print version ISSN 0365-0596

Abstract

LIMA, Alexandre Moretti de et al. Case for diagnosis. An. Bras. Dermatol. [online]. 2011, vol.86, n.1, pp. 165-166. ISSN 0365-0596.  http://dx.doi.org/10.1590/S0365-05962011000100030.

Steatocystoma multiplex is a rare genetic disorder, autosomal dominant, that is characterized by multiple asymptomatic dermal cysts which vary in size. It is described here the case of a 23 year-old male patient with a typical clinical and evolutional progression of this disease.

Keywords : Cysts; Mutation; Keratin-17.

        · abstract in Portuguese     · text in English | Portuguese     · pdf in English | Portuguese