Literature DB >> 3977245

Cherubism.

R Riefkohl, G S Georgiade, N G Georgiade.   

Abstract

Cherubism is a rare, hereditary fibroosseous lesion of the jaws that is thought to undergo spontaneous involution after puberty. Treatment is unnecessary unless functional or emotional disturbances develop. This article describes the 21-year follow-up of a patient with cherubism and briefly reviews the pertinent literature.

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Year:  1985        PMID： 3977245     DOI： 10.1097/00000637-198501000-00016

Source DB:  PubMed          Journal:  Ann Plast Surg        ISSN： 0148-7043            Impact factor:   1.539


  3 in total

1.  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

2.  Study of the cell biology and biochemistry of cherubism.

Authors:  J Southgate; U Sarma; J V Townend; J Barron; A M Flanagan
Journal:  J Clin Pathol       Date:  1998-11       Impact factor: 3.411

3.  Cherubism: A Rare Fibro-Osseous Disorder Characterized and Diagnosed by one Stop Imaging with Technetium-99m Methylene Diphosphonate Bone Scintigraphy Integrated with Single-Photon Emission Computed Tomography-Computed Tomography.

Authors:  Jaykanth Amalachandran; Thangalakshmi Sivathapandi; Shelley Simon; Indirani Elangoven; Patel Asra; Nikita S Rao; Meetashree Nayak
Journal:  Indian J Nucl Med       Date:  2019 Jan-Mar
  3 in total

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