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Isolated sternocostoclavicular hyperostosis

MONDO:0044355

Isolated sternocostoclavicular hyperostosis is a rare rheumatologic disease characterized by predominantly bilateral, chronic, sterile inflammation and progressive sclerosis and hyperostosis of the sternocostoclavicular joint, with adjacent soft tissue ossification, in the absence of other joint involvement. It presents as recurrent episodes of pain, edema and/or erythema of the sternoclavicular region. Palmoplantar pustulosis may be additionally observed in some cases.

Also known as: isolated SCCH

0 clinical trials for this condition and its sub-types, 0 tagged with Isolated sternocostoclavicular hyperostosis itself.

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