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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Galenos Publishing
2011
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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 |