Vascular flora of the cerrado of Bauru-SP

Information on the cerrado vascular flora of the municipality of Bauru has been provided in lists of floristic surveys carried out in fragments of this vegetation type at different times, applying different criteria, and conforming to current taxonomic classifications. We organized this information according to APG III and revised synonymies, aiming at producing a single floristic list of species occurring in cerrado sensu lato or ecotonal areas (transitions between cerrado and seasonal forest) in municipality of Bauru to inform conservation proposals. For this purpose, we referred to all floristic lists of vascular plants found in cerrado fragments in Bauru and to botanic material collected and deposited in the herbaria of the Department of Biological Sciences, School of Sciences, Bauru Campus, UNESP (UNBA), and of the Bauru Botanical Garden (JBMB). We recorded 371 species from 78 families. Fabaceae was the richest in species. We also indicated each mentioned species’ habit and the vegetation types where plants occur in the municipality

Fibrodisplasia ossificante progressiva: relato de caso e achados radiográficos Fibrodysplasia ossificans progressiva: a case report and radiographic findings

A fibrodisplasia ossificante progressiva é uma doença genética rara do tecido conjuntivo, caracterizada por ossificação disseminada em tecidos moles e alterações congênitas das extremidades. Sua transmissão é autossômica dominante, com penetrância completa, mas expressão variável. O início ocorre na infância e o envolvimento progressivo axial e da região proximal dos membros leva a uma conseqüente imobilização e deformação articular. Apresentamos um caso de um paciente de 22 anos de idade, do sexo masculino, com quadro clínico característico de fibrodisplasia ossificante progressiva e discutimos os últimos avanços no diagnóstico e na fisiopatogenia desta entidade.<br>Fibrodysplasia ossificans progressiva is a rare hereditary connective tissue disease characterized by disseminated soft tissue ossification and congenital abnormality of the extremities. It is genetically inherited as a dominant trait with complete penetrance but variable expression. The onset takes place during childhood and the progressive involvement of the spine and proximal extremities leads to immobilization and articular deformity. We report a case of a 22-year-old male patient with typical symptoms of fibrodysplasia ossificans progressiva and discuss the new advances in the diagnosis and pathophysiology