Abstract
ejd.2011.1528 Auteur(s) : Maria Joao Cruz1 mjmc@live.com.pt, Teresa Baudrier1, Maria Joao Gil-Da-Costa2, Filomena Azevedo1, Alberto Mota1,3 1 Department of Dermatology and Venereology 2 Department of Pediatric Hematoncology. Hospital Sao Joao, Alameda Prof. Hernani Monteiro, 4202-451 Porto, Portugal 3 Faculty of Medicine, Porto, Portugal Neurofibromatosis type 2 (NF2) is an autosomal dominant disorder caused by mutations in a tumor suppressor gene located on chromosome 22q12. The average age [...]
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