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Split hand, unilateral is a rare, non-syndromic limb reduction defect, clinically and genetically heterogeneous, characterized by unilateral underdevelopment or absence of the central rays of the autopod, with absence of all, or just some, of the central phalanges and at least part of the associated metacarpal bones, yielding a cleft appearance of the hand. It is frequently associated with syndactyly and aplasia/hypoplasia of remaining digits and metacarpal bones. No other dysmorphic features are observed and development is appropriate for age.
Biomarker and diagnostic research for split hand, unilateral has been reported in the published literature.
No clinical trials have been registered for split hand, unilateral.
5 publications have been identified in PubMed for split hand, unilateral. Research spans Diagnostic / Biomarker (40%), Clinical Trial Publication (40%), and Case Report / Case Series (20%).
Wang B (2026). [PMID: 42051705](https://pubmed.ncbi.nlm.nih.gov/42051705/). *Front Med (Lausanne)*. [Diagnostic / Biomarker]
Farvardin H (2025). [PMID: 39620612](https://pubmed.ncbi.nlm.nih.gov/39620612/). *J Pediatr Ophthalmol Strabismus*. [Clinical Trial Publication]
Yaman A (2025). [PMID: 40270640](https://pubmed.ncbi.nlm.nih.gov/40270640/). *Turk J Phys Med Rehabil*. [Clinical Trial Publication]
Ismiarto YD (2025). [PMID: 39809051](https://pubmed.ncbi.nlm.nih.gov/39809051/). *Int J Surg Case Rep*. [Case Report / Case Series]
Zeybek SG (2024). [PMID: 38494584](https://pubmed.ncbi.nlm.nih.gov/38494584/). *Int Urol Nephrol*. [Diagnostic / Biomarker]
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 11:52 AM UTC
European rare disease database