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eyebrow duplication-syndactyly syndrome - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

eyebrow duplication-syndactyly syndrome

MONDO:0009200

Also known as:eyebrows duplication of, with stretchable skin and syndactylyeyebrows, DUPLICATION of, with stretchable skin and syndactyly

Overview

Eyebrow duplication-syndactyly syndrome is characterized by partial duplication of the eyebrows and syndactyly of the fingers and toes. It has been described in three patients (a brother and sister and an isolated case). Skin hyperelasticity, hypertrichosis and long eyelashes, and abnormal periorbital wrinkling were also reported in some of the patients. Transmission is autosomal recessive.

Prognosis

Estimated prevalence: <1 in 1,000,000 (VERY_RARE).

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 eyebrow duplication-syndactyly syndrome.

102 publications have been identified in PubMed for eyebrow duplication-syndactyly syndrome. Kisho has analyzed 79 by research type. Research spans Case Report / Case Series (61%), Basic Science / Preclinical (11%), and Review / Meta-Analysis (10%).

Research Type	Count	% of Total
Patient case studies	48	61%

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 5:37 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:227210

Orphanet

European rare disease database

Orphanet:3172

GARD

Genetic and Rare Diseases Info Center

GARD:2216

Questions for Your Care Team

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eyebrow duplication-syndactyly syndrome

Overview

Prognosis

Research Landscape

Medical References

External Resources

OMIM

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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