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A Case Report of Familial Osteopoikilosis

Yune SH, Lee JK, Ahn SR, Rha SY, Park CH

Osteopoikilosis is an asymptomatic osteosclerotic dysplasia, initially described by Albers-Schönberg and Ledoux-Lebard and associates. This disorder is described as extremely rare. Inherited and sporadic cases of osteopopikilosis have been reported....
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Osteopoikilosis: A Case Report

Lee EW, Kang JW, Jung KY

Osteopoikilosis is a familial, rare condition only discovered on radiological examination for a coincident disease. It is characterized by numerous nodules of dense bone in the spongiosa of the metaphysis...
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Innumerable Small Bony Nodular Sclerotic Lesions with Negative Findings on Both Bone Scintigraphy and F-18 FDG PET : Osteopoikilosis in a Patient of Breast Cancer

Jun S, Kim YK, Kim IJ, Nam HY, Kim BS

  • KMID: 2313050
  • Nucl Med Mol Imaging.
  • 2008 Jun;42(3):256-258.
Osteopoikilosis is a rare, benign hereditary disease, which presents multiple osteosclerotic, and small round nodules in the bone. It is usually detected incidentally by radiological examination. A radionuclide bone scintigraphy...
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Non-Familial Osteopoikilosis around the both Hip Joints: a Case Report

Yoo JH, Park YW, Park JS, Rowe KC, Chung KJ, Kim HK, Song YS, Hwang JH

Osteopoikilosis is an osteosclerotic dysplasia of an unknown origin, and this malady is both extremely rare and hereditary and sporadic in nature. It is sometimes asymptomatic and incidentally diagnosed with...
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Buschke-Ollendorff Syndrome: A Case Report

Kim BS, Lee ES, Won YY, Kim HJ, Joo HJ, Han KJ, Ahn JI

The osteopoikilosis is commonly known as harmatoma in which metaphyseal and epiphyseal area of long bones and the bone of pelvis, hands, feet and et al, contain islands of dense...
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Osteopoikilosis: Report of 6 cases

Kim Y, Kim YI, Moon MK

Osteopoikilosis is condensing or sclerosing osteopathy which is generally believed to be congenital anomalies and heriditary in nature. Osteopoikolosis or osteopathia condensans disseminata is a condition which is ralatively rare...
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Novel 4-bp Intronic Deletion (c.1560+3_1560+6del) in LEMD3 in a Korean Patient With Osteopoikilosis

Yoo IY, Song JS, Ki CS, Kim JW, Cha HS, Min YK

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...
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