Familiar osteopoikilosis: Case report with differential diagnosis and review of the literature

Familiar osteopoikilosis: Case report with differential diagnosis and review of the literature

Abstract Osteopoikilosis (OP) is a rare autosomal dominant sclerosing bone disease, caused by heterozygous mutations in the LEMD3 gene. It is characterised by numerous focal lamellar bone compact deposits in the spongiosa. In this case report, we describe a famliar case of OP and review the literatu...

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Bibliographic Details
Main Authors: Agostino Gaudio, Anastasia Xourafa, Rosario Rapisarda, Cristina Gorgone, Maria Gnoli, Elena Pedrini, Luca Sangiorgi, Antonino Catalano, Luca Zanoli, Teresa Mattina, Pietro Castellino
Format: Article
Language:English
Published: Wiley 2021-02-01
Series:Clinical Case Reports
Subjects:
enostoses
LEMD3 gene
osteopoikilosis
sclerosing bone dysplasia
Online Access:https://doi.org/10.1002/ccr3.3611

Internet

https://doi.org/10.1002/ccr3.3611

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