Case Report
Multiple Exostosis and Embryonic Clubfoot in a
Premature Newborn: Case Report
Fernanda Martins Coelho Catharino1, Marco Orsini2*, Jacqueline Stephanie Fernandes do Nascimento3, Antonio Marcos da Silva Catharino4 and Marco Azizi5
1Post-Graduated in Pediatrics PUC-RJ, Brazil
2Iguaçu University (UNIG), Severino Sombra University (USS), Brazil
3Iguaçu University (UNIG) - Faculty of Medicine, Brazil
4Master in Neurology-UNIRIO; Titular Member of the Brazilian Academy of Neurology; Associated Professor of Neurology – UNIG; Physician at the Neurology
Service of the General Hospital of Nova Iguaçu, Brazil
5Unig University, Brazil
Corresponding Author
Antonio Marcos da Silva Catharino - Rua Gavião Peixoto
70, Sala 811 - Icaraí - Niterói - Rio de Janeiro – Brasil - CEP: 24230-100, Brazil.
Received Date: July 23, 2020; Published Date: August 24, 2020
Abstract
Multiple exostosis is an inherited, autosomal dominant
condition, characterized by multiple cartilaginous lesions,
developed from the metaphysis of long bones, mainly in the
proximal and distal regions of the femur [1].
