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Dental and craniofacial characteristics in a patient with Dubowitz syndrome: a case report
INTRODUCTION: Dubowitz syndrome is a very rare, autosomal recessive disease characterized by microcephaly, growth retardation, a high sloping forehead, facial asymmetry, blepharophimosis, sparse hair and eyebrows, low-set ears and mental retardation. Symptoms vary between patients, but other charact...
| Autores principales: | , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2011
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3039604/ https://www.ncbi.nlm.nih.gov/pubmed/21272302 http://dx.doi.org/10.1186/1752-1947-5-38 |