A rare photodermatosis characterized by cutaneous photosensitivity and slight dyspigmentation without an increased risk of developing skin tumors. Telangiectasia may also be observed but no other clinical abnormalities. Patients present in infancy or childhood mode of inheritance is autosomal recessive.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version March 2024
Newly diagnosed with
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