Cathcart Charles, Hanley Tessa, Gossan Nicole, Anderson Emily, Thompson Ben
Department of Dermatology, Broadgreen Hospital, Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK.
North West Genomics Laboratory Hub, St Mary's Hospital, Manchester, UK.
Clin Exp Dermatol. 2022 May;47(5):1010-1012. doi: 10.1111/ced.15085. Epub 2022 Feb 1.
Prolidase deficiency is a rare cause of chronic ulceration with less than 100 reported cases in the literature. This article highlights to clinicians the features of this uncommon genodermatosis, the challenge of diagnosis, and treatment options.
脯氨肽酶缺乏症是慢性溃疡的罕见病因，文献报道的病例不足100例。本文向临床医生重点介绍了这种罕见遗传性皮肤病的特征、诊断挑战及治疗选择。
