Dowling–Degos disease in a 23-year-old Jordanian male: a case report

Abstract Background Dowling–Degos disease is a rare genodermatosis disorder that presents as an autosomal dominant trait during late childhood or in adolescence and is also known as reticulate pigmented anomaly of flexures, Dowling–Degos–Kitamura, or dark dot disease. Dowling–Degos disease is charac...

Full description

Saved in:
Bibliographic Details
Main Authors: Hamdah Hanifa, Aya Mohannad Hamdan, Ansam Zakaria Baniamer, Jihan Mohammed Muhaidat, Sultan Hussein Al-Sahoud, Mohammad Raed AlGhzawi, Mohammad Tareq Alfaqeh
Format: Article
Language:English
Published: BMC 2025-07-01
Series:Journal of Medical Case Reports
Subjects:
Online Access:https://doi.org/10.1186/s13256-025-05398-6
Tags: Add Tag
No Tags, Be the first to tag this record!