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- W2143200418 abstract "De Sanctis–Cacchione (DSC) syndrome is one of the rarest, most severe forms of xeroderma pigmentosum (XP). These patients with XP are of short stature, have mental disabilities, and develop progressive neurologic degeneration because of a severe inability to repair damaged DNA. Herein, we will present the case of a 9-year-old boy who had DSC syndrome with microcephaly, severe psychomotor retardation, ataxia, and hearing loss. The cutaneous manifestations included giant squamous cell carcinoma (SCC) that covered the eye, multiple facial SCCs, and pigment changes on sun-exposed areas. In addition, we include a review of reported rare cases and a brief discussion of disease management." @default.
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- W2143200418 date "2015-08-01" @default.
- W2143200418 modified "2023-10-14" @default.
- W2143200418 title "De Sanctis–Cacchione syndrome: A case report and literature review" @default.
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- W2143200418 doi "https://doi.org/10.1016/j.ijwd.2015.05.003" @default.
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