Angiokeratoma corporis diffusum without systemic features in a young Kashmiri female: a rare occurrence
JPAD-Journal of Pakistan Association of Dermatologists. 2013; 23 (3): 327-330
em Inglês
| IMEMR
| ID: emr-142946
ABSTRACT
Angiokeratoma corporis diffusum [ACD] is a variety of angiokeratoma, characterized by diffuse cutaneous hyperkeratotic vascular lesions. ACD is usually associated with many lysosomal enzyme deficiencies, though it is not a rule. It is associated with systemic features along with skin lesions. It may also present as isolated cutaneous form. X-linked recessive form usually manifests in males and females act as carriers. We report a case of ACD without systemic features in a young Kashmiri female.
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Índice:
IMEMR (Mediterrâneo Oriental)
Assunto principal:
Doenças por Armazenamento dos Lisossomos
/
Doença de Fabry
/
Alfa-L-Fucosidase
/
Angioceratoma
Tipo de estudo:
Relato de Casos
Limite:
Feminino
/
Humanos
Idioma:
Inglês
Revista:
J. Pak. Assoc. Dermatol.
Ano de publicação:
2013
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