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

• Egile Nagusiak: Patricia Moraes Resende de Jesus (Egilea), Ana Maria Martins (Egilea), Nilton Di Chiacchio (Egilea), Carolina Sanchez Aranda (Egilea)
• Formatua: Liburua
• Argitaratua: Sociedade Brasileira de Dermatologia, 2018-06-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: 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...