A rare cause of cutaneous ulceration: Prolidase deficiency
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DOI: 10.1111/iwj.13138
Abstract: Dear Editors, Prolidase deficiency (PD) is a rare hereditary disease characterised by skin lesions including ulcerations, frequent infections, characteristic facies, mental retardation, and splenomegaly. Diagnosis of prolidase activity is made by sequence analysis of the… read more here.
Keywords: pepd gene; prolidase deficiency; prolidase; ulceration ... See more keywords