Literature DB >> 11728115

Cherubism and its charlatans.

D A Lannon1, M J Earley.   

Abstract

Cherubism is a rare hereditary condition characterised by progressive cystic proliferation of the mandible and maxilla in childhood, followed by post-pubertal involution of the process and jaw remodelling in adulthood. Its name is derived from the cherubic appearance that results from the jaw hypertrophy. Here, we present the case of a young boy with cherubism, in the context of his pedigree, to illustrate the clinical characteristics and their variable expression. We also seek to distinguish cherubism from central giant cell granuloma and giant cell tumour of the jaws, with which it holds a false synonymity. Copyright 2001 The British Association of Plastic Surgeons.

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Year:  2001        PMID: 11728115     DOI: 10.1054/bjps.2001.3701

Source DB:  PubMed          Journal:  Br J Plast Surg        ISSN: 0007-1226


  17 in total

1.  SH3BP2 mutations potentiate osteoclastogenesis via PLCγ.

Authors:  Steven A Lietman; Lihong Yin; Michael A Levine
Journal:  J Orthop Res       Date:  2010-11       Impact factor: 3.494

2.  Cherubism: a case report.

Authors:  Saikrishna Degala; K P Mahesh
Journal:  J Maxillofac Oral Surg       Date:  2013-02-24

3.  Role of osteoclasts in oral homeostasis and jawbone diseases.

Authors:  Maiko Omi; Yuji Mishina
Journal:  Oral Sci Int       Date:  2020-07-21

Review 4.  Benign fibro-osseous lesions of the craniofacial complex. A review.

Authors:  Roy Eversole; Lan Su; Samir ElMofty
Journal:  Head Neck Pathol       Date:  2008-05-13

5.  Bone marrow transplantation improves autoinflammation and inflammatory bone loss in SH3BP2 knock-in cherubism mice.

Authors:  Teruhito Yoshitaka; Mizuho Kittaka; Shu Ishida; Noriyoshi Mizuno; Tomoyuki Mukai; Yasuyoshi Ueki
Journal:  Bone       Date:  2014-10-31       Impact factor: 4.398

6.  Cherubism combined with epilepsy, mental retardation and gingival fibromatosis (Ramon syndrome): a case report.

Authors:  J Suhanya; Chakshu Aggarwal; Khadijah Mohideen; S Jayachandran; I Ponniah
Journal:  Head Neck Pathol       Date:  2009-12-11

7.  SH3BP2 is an activator of NFAT activity and osteoclastogenesis.

Authors:  Steven A Lietman; Lihong Yin; Michael A Levine
Journal:  Biochem Biophys Res Commun       Date:  2008-04-25       Impact factor: 3.575

Review 8.  Rare Diseases of the Orbit.

Authors:  Ulrich Kisser; Jens Heichel; Alexander Glien
Journal:  Laryngorhinootologie       Date:  2021-04-30       Impact factor: 1.057

Review 9.  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

10.  Clinical and radiological features of nonfamilial cherubism: A case report.

Authors:  Justyna Wagel; Klaudiusz Luczak; Barbara Hendrich; Maciej Guziński; Marek Sąsiadek
Journal:  Pol J Radiol       Date:  2012-07
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