familial clubfoot due to 17q23.1q23.2 microduplication
ORPHA: 238578
Overview
17q23.1-q23.2 microduplication is a newly described cause of familial isolated clubfoot.
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with familial clubfoot due to 17q23.1q23.2 microduplication, sourced from HPO and Orphanet clinical annotations.
Hip dysplasiaTalipes equinovarusHypoplastic toenailsShort stature
Classification & Codes
Orphanet Code
ORPHA:238578familial clubfoot due to 17q23.1q23.2 microduplication
| Orphanet | ORPHA:238578 |
| Treatments | 0 drug(s) |
| Symptoms on record | 4 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO