The delta phalanx, also known as a longitudinal epiphyseal bracket or clinodactyly with delta phalanx, is an uncommon deformity of the proximal phalanges and metacarpals. It is usually diagnosed by ~24 months of age, as restricted growth and angular deformities become evident. The defect is caused by a C-shaped secondary bone growth that extends along one side of the diaphysis, making straight longitudinal growth impossible. Curvature of the diaphysis and metaphysis produces a trapezoidal middle phalanx leading to angulation of the distal phalanx. The defect is also classified as Type III clinodactyly.1,3,5
Pathophysiology
- Affects fingers more commonly than toes; most common in the proximal phalanx of the thumb and middle phalanx of the little finger
- Caused by secondary center of ossification in aberrant epiphysis
- Proximal-to-distal ossification causes unequal longitudinal growth of diaphysis, which is characterized by a triangular- or trapezoidal-shaped bone with a C-shaped epiphyseal plate, as the epiphysis curves from a normal transverse to a longitudinal orientation
- Delta phalanges usually occur bilaterally.
- The mode of inheritance is thought to be autosomal dominant with incomplete penetrance.3
Related Anatomy
- Proximal, Middle and Distal Phalanges
- Metacarpals
- Epiphyseal plate
- Diaphysis of the middle phalanx
Incidence and Related Conditions
- Delta phalanx is slightly more common in males than females.3
- Clinodactyly in North America occurs at a rate of 1in 1000.4
- Associated with numerous rare syndromes including:
- Rubinstein-Taybi syndrome
- Cenani-Lenz syndactyly
- Isolated oligosyndactyly
- Nievergelt syndrome syndactyly
- Symphalangism
- Triphalangeal thumb
- Cleft hand
- Hypoplastic hand
- Apert's syndrome (index finger)
- Poland's syndrome
- Clinodactyly with no delta phalanx
- Polydactyly
Differential Diagnosis
- Type I clinodactyly
- Type II clinodactyly
- Camptodactyly
- Kirner's deformity 2