Multicentric osteolysis, nodulosis, and arthropathy

A rare, autosomal recessive inherited syndrome caused by mutations in the MMP2 gene. It is characterized by the presence of multiple, painless subcutaneous nodules, osteolysis particularly in the hands and feet, osteoporosis, and arthropathy.

Also known as: Al-Aqeel Sewairi syndrome, MONA, MONA, MMP2-related, NAO syndrome, Torg syndrome, Winchester-Torg syndrome, multicentric osteolysis, nodulosis and arthropathy, MMP2-related, multicentric osteolysis, nodulosis, and arthropathy

0 clinical trials for this condition and its sub-types.