Literature DB >> 24005878

Genetic study of an Indian family with cherubism.

Ankur Singh1, Khushbu Singh, Ruchi Goel, Ying Hu, Ernst Reichenberger, Seema Kapoor.   

Abstract

Cherubism (OMIM : 118400) is an autosomal dominant disorder affecting mainly facial bones leading to disfigurement of face needing medical and surgical attention besides impairing the self esteem of person. At present, there is no medical cure and there is limited indication for surgery in such cases. So, correct diagnosis is of paramount importance to both treating physician and family. Here, the authors report a family with two affected members (mother and daughter) who were tested positive for a known pathogenic mutation and thus offered timely treatment and adequate genetic counseling.

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Year:  2013        PMID: 24005878     DOI: 10.1007/s12098-013-1195-4

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  9 in total

1.  The gene for cherubism maps to chromosome 4p16.

Authors:  V Tiziani; E Reichenberger; C L Buzzo; S Niazi; N Fukai; M Stiller; H Peters; F M Salzano; C M Raposo do Amaral; B R Olsen
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

Review 2.  Cherubism: a 36-year long-term follow-up of 2 generations in different families and review of the literature.

Authors:  N Von Wowern
Journal:  Oral Surg Oral Med Oral Pathol Oral Radiol Endod       Date:  2000-12

3.  Identical Mutation in SH3BP2 Gene Causes Clinical Phenotypes with Different Severity in Mother and Daughter - Case Report.

Authors:  L Preda; O Dinca; A Bucur; C Dragomir; E Severin
Journal:  Mol Syndromol       Date:  2010-06-09

4.  A novel c.1255G>T (p.D419Y) mutation in SH3BP2 gene causes cherubism in a Turkish family.

Authors:  Nuriye Dinckan; Yeliz Guven; Hulya Kayserili; Oya Aktoren; Oya Zehra Uyguner
Journal:  Oral Surg Oral Med Oral Pathol Oral Radiol       Date:  2012-05-12

5.  The gene for cherubism maps to chromosome 4p16.3.

Authors:  J Mangion; N Rahman; S Edkins; R Barfoot; T Nguyen; A Sigurdsson; J V Townend; D R Fitzpatrick; A M Flanagan; M R Stratton
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

6.  Anti-tumor necrosis factor treatment in cherubism--clinical, radiological and histological findings in two children.

Authors:  M Hero; A Suomalainen; J Hagström; P Stoor; R Kontio; H Alapulli; S Arte; S Toiviainen-Salo; P Lahdenne; O Mäkitie
Journal:  Bone       Date:  2012-10-12       Impact factor: 4.398

7.  Novel mutation in the gene encoding c-Abl-binding protein SH3BP2 causes cherubism.

Authors:  Bryan Lo; M Faiyaz-Ul-Haque; S Kennedy; R Aviv; L-C Tsui; Ahmad S Teebi
Journal:  Am J Med Genet A       Date:  2003-08-15       Impact factor: 2.802

Review 8.  Cherubism: best clinical practice.

Authors:  Maria E Papadaki; Steven A Lietman; Michael A Levine; Bjorn R Olsen; Leonard B Kaban; Ernst J Reichenberger
Journal:  Orphanet J Rare Dis       Date:  2012-05-24       Impact factor: 4.123

Review 9.  The role of SH3BP2 in the pathophysiology of cherubism.

Authors:  Ernst J Reichenberger; Michael A Levine; Bjorn R Olsen; Maria E Papadaki; Steven A Lietman
Journal:  Orphanet J Rare Dis       Date:  2012-05-24       Impact factor: 4.123

  9 in total
  1 in total

1.  Unusual Characteristics and Variable Expressivity in a Brazilian Family with Cherubism.

Authors:  Desirée Deconte; Elisa Pacheco Estima Correia; Géssica Haubert; Vinicius de Souza; Jamile Dutra Correia; Marcia Angelica Peter Maahs; Paulo Ricardo Gazzola Zen; Marilu Fiegenbaum; Rafael Fabiano Machado Rosa
Journal:  J Pediatr Genet       Date:  2020-02-28
  1 in total

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