{Reference Type}: Case Reports
{Title}: Familiar osteopoikilosis: Case report with differential diagnosis and review of the literature.
{Author}: Gaudio A;Xourafa A;Rapisarda R;Gorgone C;Gnoli M;Pedrini E;Sangiorgi L;Catalano A;Zanoli L;Mattina T;Castellino P;
{Journal}: Clin Case Rep
{Volume}: 9
{Issue}: 2
{Year}: Feb 2021
暂无{DOI}: 10.1002/ccr3.3611
{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 literature.