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Pediatr Dent ; 34(5): 144-7, 2012.
Article in English | MEDLINE | ID: mdl-23211900

ABSTRACT

The purpose of this report was to: summarize the care of a child between the ages of 12 to 16 years old born with Noonan-like central giant cell syndrome and unrelated common variable immune deficiency; provide information on the dental management of patients with Noonan's syndrome; and present a brief discussion of the recent associated genetic findings. A review of the common features of Noonan syndrome and Noonan-like central giant cell syndrome is also provided.


Subject(s)
Common Variable Immunodeficiency/complications , Dental Care for Chronically Ill , Granuloma, Giant Cell/etiology , Mandibular Diseases/etiology , Noonan Syndrome/complications , Child , Female , Granuloma, Giant Cell/complications , Granuloma, Giant Cell/diagnostic imaging , Granuloma, Giant Cell/genetics , Granuloma, Giant Cell/surgery , Humans , Malocclusion/etiology , Mandibular Diseases/complications , Mandibular Diseases/diagnostic imaging , Mandibular Diseases/surgery , Noonan Syndrome/diagnostic imaging , Noonan Syndrome/genetics , Noonan Syndrome/surgery , Orthodontics, Corrective , Protein Tyrosine Phosphatase, Non-Receptor Type 11/genetics , Radiography , Tooth Abnormalities/etiology
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