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Stanescu type dysostosis is a rare form of osteosclerosis.
Biomarker and diagnostic research for dysostosis, Stanescu type has been reported in the published literature.
Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for dysostosis, Stanescu type.
9 publications have been identified in PubMed for dysostosis, Stanescu type. Research spans Case Report / Case Series (44%), Basic Science / Preclinical (22%), and Diagnostic / Biomarker (11%).
Esener Z (2025). [PMID: 40358131](https://pubmed.ncbi.nlm.nih.gov/40358131/). *Am J Med Genet A*. [Case Report / Case Series]
Laaraje A (2025). [PMID: 41693193](https://pubmed.ncbi.nlm.nih.gov/41693193/). *Pediatr Endocrinol Diabetes Metab*. [Case Report / Case Series]
Ranjitkar S (2025). [PMID: 40088245](https://pubmed.ncbi.nlm.nih.gov/40088245/). *Am J Orthod Dentofacial Orthop*. [Diagnostic / Biomarker]
Hegab AF (2025). [PMID: 41023115](https://pubmed.ncbi.nlm.nih.gov/41023115/). *Sci Rep*. [Epidemiology / Natural History]
Ozturk M (2025). [PMID: 40898781](https://pubmed.ncbi.nlm.nih.gov/40898781/). *Dev Neurobiol*. [Case Report / Case Series]
Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 11:55 PM UTC
Online Mendelian Inheritance in Man
European rare disease database
Genetic and Rare Diseases Info Center
Zheng Y (2024). [PMID: 39048474](https://pubmed.ncbi.nlm.nih.gov/39048474/). *Differentiation*. [Review / Meta-Analysis]
Gu Y (2024). [PMID: 39087232](https://pubmed.ncbi.nlm.nih.gov/39087232/). *J Clin Pediatr Dent*. [Case Report / Case Series]
Chen D (2024). [PMID: 38372889](https://pubmed.ncbi.nlm.nih.gov/38372889/). *Hum Cell*. [Basic Science / Preclinical]