Shprintzen-goldberg craniosynostosis: craniofacial and oral characteristics, diagnosis, and clinical management of a very rare syndrome

• Autores principales: Danielle Monsores VIEIRA (Autor), Florense Gabriela SILVA (Autor), Michele Baffi DINIZ (Autor), Maria Cristina Duarte FERREIRA (Autor), Maria Teresa Botti Rodrigues dos SANTOS (Autor), Renata Oliveira GUARÉ (Autor)
• Formato: Libro
• Publicado: Faculdade São Leopoldo Mandic, 2022-10-01T00:00:00Z.
• Materias: article
• Acceso en línea: Connect to this object online.

ABSTRACT Shprintzen-Goldberg craniosynostosis syndrome, characterized by craniosynostosis and marfanoid habitus, is a very rare entity described in 75 individuals worldwide. This study aimed to present a case report of a 6-year-old female Brazilian child with Shprintzen-Goldberg's craniosynosto...