| Literature DB >> 31129707 |
Maria Gnoli1, Eric Lodewijk Staals2, Laura Campanacci2, Maria Francesca Bedeschi3, Flavio Faletra4, Salvatore Gallone5, Agostino Gaudio6, Teresa Mattina7, Fiorella Gurrieri8, Antonio Percesepe9, Iria Neri10, Annalucia Virdi10, Morena Tremosini11, Annamaria Milanesi11, Evelise Brizola11, Elena Pedrini11, Luca Sangiorgi12.
Abstract
Melorheostosis (MEL) is an uncommon, sclerosing disease, characterised by hyperostosis of long bones, resembling the flowing of candle wax. The disease is sporadic and the pathogenesis is still poorly understood. Occasionally, the same family can include individuals with MEL and Osteopoikilosis (OPK), a disease characterised by multiple round foci of increased bone density. LEMD3 gene mutations are related to OPK and Buschke-Ollendorff Syndrome, a genetic condition in which an association between MEL, OPK and skin lesions is observed. In rare cases, LEMD3 mutations and recently mosaic MAP2K1 gene mutations have been correlated to MEL suggesting that somatic mosaicism could be causative of the disease. In this study, we described the clinical, radiological and molecular findings of 19 individuals with MEL and 8 with OPK and compared the results to the medical literature. The molecular analyses of this case series corroborate the available data in the medical literature, indicating that LEMD3 germline mutations are not a major cause of isolated MEL and reporting five further cases of OPK caused by LEMD3 germline mutations.Entities:
Keywords: LEMD3 gene; Melorheostosis; Osteopoikilosis; Osteopoikilosis with or without melorheostosis
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Year: 2019 PMID: 31129707 DOI: 10.1007/s00223-019-00565-6
Source DB: PubMed Journal: Calcif Tissue Int ISSN: 0171-967X Impact factor: 4.333