Literature DB >> 22524084

Atypical orofacial conditions in Noonan syndrome: a case report.

Leo Toureno1, Jae Hyun Park.   

Abstract

Noonan syndrome (NS) is a relatively common condition characterized by chest deformation, congenital heart disease, short stature and distinctive facial features. Due to its genetic heterogeneity NS patients exhibit a range of clinical signs. Severe gingivitis and supernumerary teeth are rarely seen in connection with NS. In addition, there has not been a report on NS patients with atypical bilateral enlargement of the mental foramens and inferior-alveolar canals. This case report describes a NS patient who has undergone growth hormone (GH) therapy and is presenting with classical and rare NS phenotypes.

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Year:  2011        PMID: 22524084     DOI: 10.17796/jcpd.36.2.81074271088334h2

Source DB:  PubMed          Journal:  J Clin Pediatr Dent        ISSN: 1053-4628            Impact factor:   1.065


  3 in total

1.  Sequential Loss of Mandibular Permanent Incisors in Noonan Syndrome.

Authors:  Reinhard E Friedrich; Hanna A Scheuer
Journal:  In Vivo       Date:  2022 Mar-Apr       Impact factor: 2.155

Review 2.  Odontomas and supernumerary teeth: is there a common origin?

Authors:  Roberto Pippi
Journal:  Int J Med Sci       Date:  2014-11-12       Impact factor: 3.738

3.  Multiple Unerupted Permanent Teeth Associated with Noonan Syndrome.

Authors:  K S Uloopi; V Madhuri; A S Gopal; C Vinay; R Chandrasekhar
Journal:  Ann Med Health Sci Res       Date:  2015 Jul-Aug
  3 in total

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