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J Clin Pediatr Dent ; 37(2): 203-6, 2012.
Article in English | MEDLINE | ID: mdl-23534331

ABSTRACT

Dubowitz syndrome is a rare genetic condition characterized by microcephaly, dysmorphic facial features and delayed general growth. It is transmitted through autosomal recessive inheritance. The purpose of this report is to describe the oral, craniofacial and systemic characteristics of a 7-year 11-month-old boy with Dubowitz syndrome and the dental management provided. The pediatric dentist should possess the ability to recognize this rare alteration, to provide dental treatment and to refer for the necessary medical and multidisciplinary treatment.


Subject(s)
Dental Caries/therapy , Dental Restoration, Permanent/methods , Eczema/complications , Growth Disorders/complications , Intellectual Disability/complications , Microcephaly/complications , Airway Obstruction/etiology , Cephalometry , Child , Dental Caries/etiology , Facial Bones/abnormalities , Facies , Humans , Hypertelorism/etiology , Male , Malocclusion/etiology , Micrognathism/etiology , Open Bite/etiology , Pit and Fissure Sealants/therapeutic use , Retrognathia/etiology , Syndrome
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