acropectoral syndrome
Findings
No curated finding names acropectoral syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Acro-pectoral syndrome is characterized by a combination of distal limb abnormalities (syndactyly of all fingers and toes, preaxial polydactyly in the feet and/or hands) and upper sternum malformations. It has been described in 22 patients from a six-generation Turkish family. It is transmitted as an autosomal dominant trait and the causative gene is located at 7q36.
Definition from the Mondo Disease Ontology (MONDO:0011621), read 2026-09-29. CC BY 4.0.
Features
3 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Abnormal thorax morphologyHPOHP:0000765
- Very frequent (80% to 99% of cases)
- Finger syndactylyHPOHP:0006101
- Very frequent (80% to 99% of cases)
- Preaxial hand polydactylyHPOHP:0001177
- Very frequent (80% to 99% of cases)
Where it sits
Other names
2 names
Resolves to: acropectoral syndrome
- Also called
- ACRP syndromesyndactyly-preaxial polydactyly-sternal deformity syndrome