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Sheldon-Hall syndrome (SHS) is a rare multiple congenital contracture syndrome characterized by contractures of the distal joints of the limbs, triangular face, downslanting palpebral fissures, small mouth, and high arched palate.
Estimated prevalence: Unknown (Unknown prevalence).
No clinical trials have been registered for Sheldon-hall syndrome.
4 publications have been identified in PubMed for Sheldon-hall syndrome. Research spans Review / Meta-Analysis (50%) and Case Report / Case Series (50%).
Umar M (2025). [PMID: 40746736](https://pubmed.ncbi.nlm.nih.gov/40746736/). *Genes Dis*. [Review / Meta-Analysis]
Chen Y (2024). [PMID: 38873579](https://pubmed.ncbi.nlm.nih.gov/38873579/). *Front Pediatr*. [Case Report / Case Series]
Illés A (2024). [PMID: 39062310](https://pubmed.ncbi.nlm.nih.gov/39062310/). *Children (Basel)*. [Review / Meta-Analysis]
Morali B (2024). [PMID: 38856159](https://pubmed.ncbi.nlm.nih.gov/38856159/). *Clin Genet*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 1:01 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about Sheldon-hall syndrome