| Literature DB >> 33552642 |
Desirée Deconte1, Elisa Pacheco Estima Correia2, Géssica Haubert2, Vinicius de Souza2, Jamile Dutra Correia1, Marcia Angelica Peter Maahs3, Paulo Ricardo Gazzola Zen1,4, Marilu Fiegenbaum1,5, Rafael Fabiano Machado Rosa1,4.
Abstract
Cherubism is a rare genetic condition characterized by a bone nonneoplastic disease. We aimed to report a 6-year-old girl with cherubism presenting similar cases in the maternal family. However, her mother and grandmother seemed to be asymptomatic. The patient had an enlarged and asymmetric jaw with multiple enlarged cervical lymph nodes that increased in size with time. Sanger sequencing revealed a heterozygous mutation in exon 9 of SH3BP2 not only in the patient but also in her mother. Thus, we observed a variable expression and a probably reduced penetrance within the family, as well as unusual characteristics of the patient (in this case, the asymmetrical involvement of the jaw). Thieme. All rights reserved.Entities:
Keywords: asymmetry; cherubism; variable expressivity
Year: 2020 PMID: 33552642 PMCID: PMC7853913 DOI: 10.1055/s-0040-1705095
Source DB: PubMed Journal: J Pediatr Genet ISSN: 2146-460X