Kindler syndrome: a rare case report from Syria.
| Autor: | Edrees S; Departments of Dermatology., Jarkas N; Departments of Dermatology., Hraib M; Faculty of Medicine, Tishreen University, Latakia, Syria., Al-Yousef K; Urology, Tishreen University Hospital., Baddour R; Departments of Dermatology. |
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| Jazyk: | angličtina |
| Zdroj: | Annals of medicine and surgery (2012) [Ann Med Surg (Lond)] 2023 Apr 06; Vol. 85 (5), pp. 2077-2080. Date of Electronic Publication: 2023 Apr 06 (Print Publication: 2023). |
| DOI: | 10.1097/MS9.0000000000000503 |
| Abstrakt: | Kindler syndrome is a rare autosomal recessive inherited disease. The authors report a case with unique presentation that has never reported before in the medical Literatur" lanugo hair". This is a case of a 13-year-old Syrian child, who presented with difuse fine face hair, and serious urinary complications. Kindler syndrome is characterized by acral skin blistering beginning at birth, diffuse cutaneous atrophy, photosensitivity, poikiloderma, and various mucosal findings. Highlighting a set of clinical diagnostic criteria; which is used only if a genetic test is not available. Competing Interests: The authors declare that there is no conflict of interest. (Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc.) |
| Databáze: | MEDLINE |
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