Title of article :
Angiokeratoma corporis diffusum without systemic features in a young Kashmiri female: a rare occurrence
Author/Authors :
Hassan, Iffat University of Kashmir - Department of Dermatology,STD Leprosy, India , Rather, Parvaiz Anwar University of Kashmir - Government Medical College - Department of Dermatology, STD Leprosy, India , Aleem, Saima University of Kashmir - Government Medical College - Department of Dermatology, STD Leprosy, India
From page :
327
To page :
330
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.
Keywords :
Angiokeratoma , angiokeratoma corporis diffusum , lysosomal enzyme deficiency.
Journal title :
Journal of Pakistan Association of Dermatologists
Journal title :
Journal of Pakistan Association of Dermatologists
Record number :
2590597
Link To Document :
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