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osteopoikilosis/dorsopatia
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6 risultati
Low back pain and osteosclerotic bone lesions suggesting metastases: mask of osteopoikilosis.
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Novel 4-bp Intronic Deletion (c.1560+3_1560+6del) in LEMD3 in a Korean Patient With Osteopoikilosis.
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Osteopoikilosis is an autosomal dominant bone disorder characterized by symmetric multiple osteosclerotic lesions throughout the axial and appendicular skeleton. Pathogenic variants in the LEMD3 have been identified as the cause of osteopoikilosis. LEMD3 encodes an inner nuclear membrane protein
Osteopoikilosis: report of a familial case and review of the literature.
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Osteopoikilosis (OPK) is a benign, rare, asymptomatic osteosclerotic bone dysplasia which is inherited as an autosomal dominant trait. It may develop during childhood and persists throughout life. Diagnosis is usually made incidentally according to radiographs. It may be confused with other
Familial osteopoikilosis.
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Osteopoikilosis (OPK) is a rare, autosomally inherited, benign sclerosing bone dysplasia of unknown etiology. It is usually found incidentally on radiological examination, presenting as multiple, small, well-defined,variably shaped and widely distributed sclerotic areas throughout the skeleton. In
Coexistence of osteopoikilosis with seronegative spondyloarthritis and spinal stenosis.
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[Purpose] Osteopoikilosis is a rare hereditary bone disease that is usually asymptomatic. It is generally diagnosed incidentally on plain radiography. The coexistence of osteopoikilosis with seronegative spondyloarthritis or spinal stenosis is rarely reported. Here, we report the case of a
Radiology and morphology of spotted bone: a case report with review of literature.
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Spotted bone disease (osteopoikilosis) is a rare type of osteosclerotic dysplasia usually noticed as an incidental finding during routine radiological investigations. Here we report a case of a male patient who had chronic history of right wrist pain and low backache. His radiographs showed unique
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