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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...
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| Päätekijät: | , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2011
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3039604/ https://ncbi.nlm.nih.gov/pubmed/21272302 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-1947-5-38 |
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