Angiokeratoma corporis diffusum

0Citations
Citations of this article
4Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Angiokeratoma is a dark violaceous keratotic papule which can be solitary or multiple. Generalised systemic angiokeratoma constitute angiokeratoma corporis diffusum, a rare X-linked recessive inborn error of glycosphingolipid metabolism due to deficiency of alpha galactosidase A. Patients with this disease have premature death due to the vascular complications. A case of possible Fabry's disease is presented.

Cite

CITATION STYLE

APA

Yap, F. B. B., & Pubalan, M. (2008). Angiokeratoma corporis diffusum. Medical Journal of Malaysia, 63(4), 329–330. https://doi.org/10.1001/archinte.1955.00250090107013

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free