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familial isolated clinodactyly of fingers - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

familial isolated clinodactyly of fingers

MONDO:0017461

Overview

Familial isolated clinodactyly of fingers is a rare, genetic, non-syndromic, congenital limb malformation characterized by angulation of a digit in the radio-ulnar (coronal) plane, away from the axis of joint flexion-extension, in several members of a single family with no other associated manifestations. Deviation is usually bilateral and commonly involves the fifth finger. Affected digits present trapezoidal or delta-shaped phalanges on imaging.

ResearchLimited published research (3 articles)

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 familial isolated clinodactyly of fingers.

3 publications have been identified in PubMed for familial isolated clinodactyly of fingers. Research spans Case Report / Case Series (67%) and Basic Science / Preclinical (33%).

Recent Publications

Ünsel-Bolat G (2025). [PMID: 40415676](https://pubmed.ncbi.nlm.nih.gov/40415676/). *Dev Neurobiol*. [Case Report / Case Series]
Lee MK (2025). [PMID: 40071514](https://pubmed.ncbi.nlm.nih.gov/40071514/). *Mol Genet Genomic Med*. [Basic Science / Preclinical]
Loukopoulos T (2024). [PMID: 39720354](https://pubmed.ncbi.nlm.nih.gov/39720354/). *Case Rep Womens Health*. [Case Report / Case Series]

Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 9:35 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:295014

GARD

Genetic and Rare Diseases Info Center

GARD:21202

Questions for Your Care Team

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familial isolated clinodactyly of fingers

Overview

Research Landscape

Recent Publications

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team