Jaffe-Campanacci syndrome or neurofibromatosis type 1: a case report of phenotypic overlap with detection of NF1 gene mutation in non-ossifying fibroma

Jaffe-Campanacci syndrome is characterized by multiple non-ossifying fibromas, caf é-au-lait macules and giant cell granulomas of the jaw. Even if the association between all these peculiar features and neurofi...

Source: Italian Journal of Pediatrics - May 11, 2020 Category: Pediatrics Authors: Silvia Vannelli, Raffaele Buganza, Federica Runfola, Ilaria Mussinatto, Antonio Andreacchio and Luisa de Sanctis Tags: Case report Source Type: research