A Case of Congenital Erythropoietic Porphyria without Hemolysis.

Abstract

Porphyrias are group of disorders caused by deficiency of the enzymes in heme synthetic pathway. Congenital erythropoietic porphyria (CEP) is an extremely rare disease with mutation in the gene that codes for uroporphyrinogen III synthase leading to accumulation of porphyrin in different tissues and marked cutaneous photosensitivity. Here, we describe a case of CEP with infancy onset blistering, photosensitivity, red colored urine and teeth along with scarring but without any feature of hemolysis.

• Authors: Arun K De, Kallol Das, Archan Sil, Swarnali Joardar
• Journal: Indian journal of dermatology (Indian J Dermatol) Vol. 58 Issue 5 Pg. 407 (Sep 2013) ISSN: 1998-3611 [Electronic] India
• PMID: 24082206 (Publication Type: Journal Article)