Literature DB >> 2033166

Williams (Elfin Facies) syndrome: review of the literature and report of a rare case.

R A Boraz1.   

Abstract

Williams (Elfin Facies) syndrome is a rare, devastating, sporadic disorder first described in 1961. Approximately 100 cases have been reported in the literature. The disorder is characterized by multiple anomalies including mental deficiency, an unusual (elfin) facies, supravalvular aortic stenosis, prenatal and postnatal growth deficiency, infantile hypercalcemia, a small mandible, and frequent dental problems. Because of these anomalies, the dentist contributes significantly to the successful management of these patients. Infant dental care, nutrition counseling, and restorative care are extremely important for maximizing the quality of life for patients with Williams syndrome. A review of the literature and the successful management of a patient with Williams syndrome are presented.

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Year:  1991        PMID: 2033166

Source DB:  PubMed          Journal:  ASDC J Dent Child        ISSN: 1945-1954


  3 in total

1.  Alternative treatment for open bite Class III malocclusion in a child with Williams-Beuren syndrome.

Authors:  Giovanni Modesto Vieira; Eduardo Jacomino Franco; Denise Falcão Pinheiro da Rocha; Laudimar Alves de Oliveira; Rivadávio Fernandes Batista Amorim
Journal:  Dental Press J Orthod       Date:  2015 Jan-Feb

2.  Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: evaluation of 235 patients.

Authors:  M C Lowery; C A Morris; A Ewart; L J Brothman; X L Zhu; C O Leonard; J C Carey; M Keating; A R Brothman
Journal:  Am J Hum Genet       Date:  1995-07       Impact factor: 11.025

3.  Dentofacial characteristics in William's syndrome.

Authors:  P Poornima; Piyusha S Patil; V V Subbareddy; Geetika Arora
Journal:  Contemp Clin Dent       Date:  2012-04
  3 in total

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