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- W1985251567 abstract "Noonan-like multiple giant cell lesion syndrome is a rare dysmorphic disorder, originally described as a distinct entity by Cohen et al in 1974, and its current name was proposed in a review of 14 cases published in 1991. Although the mode of inheritance was initially described as sporadic, there is now more evidence for an autosomal dominant inheritance, with linkage to a gene on chromosome 12. We present an aggressive case of this syndrome in a 15-year-old boy, with multiple giant cell lesions in the maxilla and mandible, which grew despite radiotherapy, antiangiogenic therapy, and high-dose steroid treatment." @default.
- W1985251567 created "2016-06-24" @default.
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- W1985251567 date "2009-12-01" @default.
- W1985251567 modified "2023-09-24" @default.
- W1985251567 title "Aggressive Noonan-Like Multiple Giant Cell Lesion Syndrome on Tc-99m MDP Bone Scan" @default.
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- W1985251567 doi "https://doi.org/10.1097/rlu.0b013e3181becf15" @default.
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