RESUMO

Ring chromosome 15 syndrome is a rare condition, with approximately 50 cases reported in the literature. We report a 2-year-old girl with ring chromosome 15 syndrome with hyperpigmented and hypopigmented patches and cognitive and physical manifestations.

Assuntos

Cromossomos Humanos Par 15/genética , Hiperpigmentação/genética , Hipopigmentação/genética , Cromossomos em Anel , Pré-Escolar , Feminino , Humanos , Cariótipo , Pele/patologia , Síndrome