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3M Syndrome: A Report of Four Cases in Two Families

3M syndrome is a rare entity characterized by severe growth retardation, dysmorphic features and skeletal changes as its major components. It is differentiated from other types of dwarfism by its clinical features and by the typical slender long bones and foreshortened vertebral bodies that can be v...

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Detalles Bibliográficos
Autores principales: Güven, Ayla, Cebeci, Ayşe Nurcan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3184518/
https://www.ncbi.nlm.nih.gov/pubmed/21911330
http://dx.doi.org/10.4274/jcrpe.v3i3.30