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.
CITATION STYLE
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
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