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Caso para diagnósticoDOI: 10.1590/S0365-05962011000100030 Keywords: cysts, mutation, keratin-17. Abstract: 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.
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