Literature DB >> 26187867

An unusual case of KBG syndrome with unique oral findings.

Abdul Hafiz1, Abdulla Mufeed2, Mohamad Ismael3, Mheboob Alam3.   

Abstract

KBG syndrome is a condition characterised by macrodontia, neurological disturbance, short stature, a distinct cranio-facial appearance, and skeletal anomalies. The authors describe what appears to be the first case of KBG syndrome reported from the Indian subcontinent. Meticulous evaluation of the dental findings helps to identify such cases which may otherwise remain undiagnosed. Further research is warranted to determine the classic and variant presentations of this condition, with follow-up data providing valuable insights into its natural history and long-term prognosis. 2015 BMJ Publishing Group Ltd.

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Mesh:

Year:  2015        PMID: 26187867      PMCID: PMC4513503          DOI: 10.1136/bcr-2015-210352

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  8 in total

1.  The KBG syndrome, characteristic dental findings: a case report.

Authors:  P A Dowling; P Fleming; R J Gorlin; M King; N C Nevin; M McEntagart
Journal:  Int J Paediatr Dent       Date:  2001-03       Impact factor: 3.455

2.  KBG syndrome: clinical features and specific dental findings.

Authors:  Abdul Hakim Almandey; Robert P Anthonappa; Nigel M King; Cheuk-wing Fung
Journal:  Pediatr Dent       Date:  2010 Sep-Oct       Impact factor: 1.874

3.  Short Stature in KBG Syndrome: First Responses to Growth Hormone Treatment.

Authors:  Nele Reynaert; C W Ockeloen; L Sävendahl; D Beckers; K Devriendt; T Kleefstra; C E L Carels; G Grigelioniene; A Nordgren; I Francois; F de Zegher; K Casteels
Journal:  Horm Res Paediatr       Date:  2015-04-01       Impact factor: 2.852

Review 4.  KBG syndrome: review of the literature and findings of 5 affected patients.

Authors:  Harleen Kumar; Neeta Prabhu; Angus Cameron
Journal:  Oral Surg Oral Med Oral Pathol Oral Radiol Endod       Date:  2009-09

5.  The KBG syndrome-a syndrome of short stature, characteristic facies, mental retardation, macrodontia and skeletal anomalies.

Authors:  J Herrmann; P D Pallister; W Tiddy; J M Opitz
Journal:  Birth Defects Orig Artic Ser       Date:  1975

6.  Mutations in ANKRD11 cause KBG syndrome, characterized by intellectual disability, skeletal malformations, and macrodontia.

Authors:  Asli Sirmaci; Michail Spiliopoulos; Francesco Brancati; Eric Powell; Duygu Duman; Alex Abrams; Guney Bademci; Emanuele Agolini; Shengru Guo; Berrin Konuk; Asli Kavaz; Susan Blanton; Maria Christina Digilio; Bruno Dallapiccola; Juan Young; Stephan Zuchner; Mustafa Tekin
Journal:  Am J Hum Genet       Date:  2011-07-21       Impact factor: 11.025

Review 7.  Taurodontism: a review of the condition and endodontic treatment challenges.

Authors:  H Jafarzadeh; A Azarpazhooh; J T Mayhall
Journal:  Int Endod J       Date:  2008-03-21       Impact factor: 5.264

8.  The KBG syndrome: Case report.

Authors:  Ilaria Morghen; Enrico Ferri
Journal:  Cases J       Date:  2008-09-26
  8 in total
  1 in total

1.  KBG syndrome involving a single-nucleotide duplication in ANKRD11.

Authors:  Robert Kleyner; Janet Malcolmson; David Tegay; Kenneth Ward; Annette Maughan; Glenn Maughan; Lesa Nelson; Kai Wang; Reid Robison; Gholson J Lyon
Journal:  Cold Spring Harb Mol Case Stud       Date:  2016-11
  1 in total

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