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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
in English | 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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Index: IMEMR (Eastern Mediterranean) Main subject: Lysosomal Storage Diseases / Fabry Disease / Alpha-L-Fucosidase / Angiokeratoma Type of study: Case report Limits: Female / Humans Language: English Journal: J. Pak. Assoc. Dermatol. Year: 2013

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Index: IMEMR (Eastern Mediterranean) Main subject: Lysosomal Storage Diseases / Fabry Disease / Alpha-L-Fucosidase / Angiokeratoma Type of study: Case report Limits: Female / Humans Language: English Journal: J. Pak. Assoc. Dermatol. Year: 2013