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isolated sternocostoclavicular hyperostosis - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

isolated sternocostoclavicular hyperostosis

MONDO:0044355

Also known as:isolated SCCH

Overview

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.

ResearchLimited published research (1 article)

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for isolated sternocostoclavicular hyperostosis.

1 publication has been identified in PubMed for isolated sternocostoclavicular hyperostosis. Research spans Review / Meta-Analysis (100%).

Recent Publications

Furer V (2024). [PMID: 39411288](https://pubmed.ncbi.nlm.nih.gov/39411288/). *Rheumatol Adv Pract*. [Review / Meta-Analysis]

Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 11:12 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:178311

GARD

Genetic and Rare Diseases Info Center

GARD:20144

Questions for Your Care Team

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isolated sternocostoclavicular hyperostosis

Overview

Research Landscape

Recent Publications

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team