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

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...

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Main Authors: Danielle Monsores VIEIRA (Author), Florense Gabriela SILVA (Author), Michele Baffi DINIZ (Author), Maria Cristina Duarte FERREIRA (Author), Maria Teresa Botti Rodrigues dos SANTOS (Author), Renata Oliveira GUARÉ (Author)
Format: Book
Published: Faculdade São Leopoldo Mandic, 2022-10-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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