Historical Overview
- The word syndactyly derives from the Greek words “syn,” together, and “daktylos,” finger.
- The first documented cases of syndactyly and polydactyly were written by Oribasius, a Byzantine physician of the 4th century.1
Description
- Syndactyly is diagnosed primarily by observation. Simple syndactyly involves fusion of the skin or tissues of fingers, whereas complex syndactyly involves fusion of bone, musculotendinous and/or neurovascular structures.2 Complete syndactyly extends to the fingertips, whereas incomplete syndactyly does not.3
- Goals of operative treatment include improved aesthetic appearance and independent function of the fingers.4
Pathophysiology
- About 80% of cases of syndactyly are sporadic. Syndactyly can also be related to conditions such as Apert’s syndrome, Poland’s syndrome, congenital constriction bands, and ectodermal dysplasia.
Instructions
- Obtain an accurate and complete patient history. Ask the parent or guardian how severely the syndactyly prevents the patient’s independent function of the fingers.3,4
- Check for insufficient amount of skin and lack of vascular supply to the affected fingers.
- Examine the involved joints, to determine if they are ankylosed, deviated, stiff, or unstable.
- Check the contralateral hand; about 50% of cases of syndactyly are bilateral.
Related Signs and Tests
- Radiographs
- Sonographic studies
Diagnostic Performance Characteristics
- Using radiographs will improve the reliability of a physical diagnosis.
Differential Diagnoses
- Apert’s syndrome
- Symbrachydactyly
- Brachysyndactyly
- Pseudosyndactyly
- Ectrodactyly
- Constriction band syndrome