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A 38-year review of oral schwannomas and neurofibromas in a Brazilian population: clinical, histopathological and immunohistochemical study

✍ Scribed by George João Ferreira do Nascimento; Danielle de Albuquerque Pires Rocha; Hébel Cavalcanti Galvão; Antônio de Lisboa Lopes Costa; Lélia Batista de Souza


Publisher
Springer
Year
2010
Tongue
English
Weight
369 KB
Volume
15
Category
Article
ISSN
1432-6981

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Bardet-Biedl syndrome (BBS) and Laurence-Moon syndrome (LMS) have a similar phenotype, which includes retinal dystrophy, obesity, and hypogenitalism. They are differentiated by the presence of spasticity and the absence of polydactyly in LMS. The aims of this study were to describe the epidemiology