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- W2077681987 abstract "Fibrodysplasia ossificans progressiva (FOP) is a rare hereditary connective tissue disease. It is genetically inherited as an autosomal dominant trait with complete penetrance but variable expressivity. Onset is typically in childhood, and progressive involvement of the spine and proximal extremities leads to immobility and articular dysfunction. A 20-year-old female appeared with jaw ankylosis due to FOP, and the pathogenesis, clinical manifestations, and treatment options of this rare disease are discussed, including a review of the literature." @default.
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- W2077681987 date "2006-09-01" @default.
- W2077681987 modified "2023-09-27" @default.
- W2077681987 title "Severe limitation in jaw movement in a patient with fibrodysplasia ossificans progressiva: a case report" @default.
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- W2077681987 doi "https://doi.org/10.1016/j.tripleo.2005.09.020" @default.
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