Genital angiokeratoma in a woman with Fabry disease: the dermatologist's role

• Váldodahkkit: Patricia Moraes Resende de Jesus (Dahkki), Ana Maria Martins (Dahkki), Nilton Di Chiacchio (Dahkki), Carolina Sanchez Aranda (Dahkki)
• Materiálatiipa: Girji
• Almmustuhtton: Sociedade Brasileira de Dermatologia, 2018-06-01T00:00:00Z.
• Fáttát: article
• Liŋkkat: Connect to this object online.

Abstract: Fabry disease is a rare lysosomal storage disorder, inherited in an X-linked manner. It is characterized by the deficiency of the enzyme alpha-galactosidase, leading to a buildup of glycosphingolipids in the cells. Angiokeratoma is one of the cutaneous manifestations of this condition, and...