Rekindle with Kindler Syndrome – Case Reports of a Rare Entity
Kindler syndrome is a rare autosomal recessive inherited disease. It is characterised by blistering in infancy, photosensitivity and progressive poikiloderma. We report a case of a 26-year-old female patient with clinical features such as acral blistering in childhood, photosensitivity and poikiloderma; confirmed by genetic testing.
Authors
- Krina Patel (ORCID: https://orcid.org/0009-0000-0949-9280)
- Drashti Pravinbhai Ramani
- Prerna Navneetbhai Patel
- Gopika Patel
Institutions
- Gujarat Cancer Society (IN)
Publication Details
- Journal
- Indian Journal of Postgraduate Dermatology
- Published
- 2026-01-02
- DOI
- https://doi.org/10.25259/ijpgd_69_2025
- Primary Topic
- Skin and Cellular Biology Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00