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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Detalles Bibliográficos
Autores principales: Ballini, Andrea, Cantore, Stefania, Tullo, Domenica, Desiate, Apollonia
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Case Report
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

Internet

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

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