Multi-directional Cranial Distraction Osteogenesis for Treating Sagittal Synostosis with Frontometaphyseal Dysplasia: A Case Report

Frontometaphyseal dysplasia (FMD), also known as Gorlin-Cohen syndrome, is a rare genetic syndrome. This syndrome affects the skeletal system and connective tissue, and causes a wide spectrum of manifestations of the skull, tubular bones, cardiovascular system, urinary system, and/or gastrointestina...

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Detalles Bibliográficos
Autores principales: Morishita, Yuya, Sunaga, Ataru, Gomi, Akira, Hatade, Alice, Morita, Yuhei, Yoshimura, Kotaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Pediatric/Craniofacial
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8078314/
https://www.ncbi.nlm.nih.gov/pubmed/33912371
http://dx.doi.org/10.1097/GOX.0000000000003551

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8078314/
https://www.ncbi.nlm.nih.gov/pubmed/33912371
http://dx.doi.org/10.1097/GOX.0000000000003551

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