Congenital Vertical Talus

Congenital Vertical Talus

Congenital Vertical Talus (CVT), also known as "rocker-bottom foot," is a rare rigid flatfoot deformity characterized by fixed dorsal dislocation of the navicular on the talus, resulting in a rigid and irreducible hindfoot valgus and forefoot dorsiflexion.

Key Characteristics:

  • Fixed dorsal navicular dislocation
  • Rigid equinus of the hindfoot
  • Forefoot dorsiflexion and abduction
  • Convex plantar surface
  • Rigidity of deformity

Epidemiology

  • Incidence: 1 in 10,000 live births
  • Bilateral in 50% of cases
  • Male:Female ratio = 1:1
  • Associated conditions in 50-90% of cases
  • Strong genetic component

Pathoanatomy

  • Key Deformities:
    • Vertically oriented talus
    • Dorsal dislocation of navicular
    • Contracture of anterior tibialis
    • Contracted dorsal capsule
    • Posterior tibialis dysfunction
  • Anatomical Changes:
    • Hindfoot equinus
    • Talonavicular dissociation
    • Forefoot dorsiflexion
    • Altered muscle balance

Clinical Presentation

  • Physical Findings:
    • Rigid rocker-bottom deformity
    • Prominent talar head plantarly
    • Deep crease on dorsum of foot
    • Fixed hindfoot equinus
    • Inability to reduce deformity
  • Key Signs:
    • Rigid deformity from birth
    • Convex plantar arch
    • Dorsal bunion appearance
    • Tight anterior tendons
    • Poor passive motion

Diagnostic Imaging

  • Radiographic Features:
    • Lateral view:
      • Vertical orientation of talus
      • Dorsal displacement of navicular
      • Parallel axes of talus and 1st metatarsal
    • AP view:
      • Forefoot abduction
      • Talar head uncoverage
      • Hindfoot valgus
  • Advanced Imaging:
    • MRI: For complex cases
    • CT: Surgical planning
    • Stress radiographs

Associated Syndromes and Conditions

  • Neuromuscular Disorders:
    • Arthrogryposis
    • Myelomeningocele
    • Sacral agenesis
    • Spinal muscular atrophy
  • Chromosomal Abnormalities:
    • Trisomy 13, 15, 18
    • De Lange syndrome
    • Down syndrome
  • Other Associations:
    • HOXD10 gene mutations
    • DiGeorge syndrome
    • Prune belly syndrome
    • Neurofibromatosis

Systemic Evaluation

  • Required Assessments:
    • Neurological examination
    • Genetic consultation
    • Spine evaluation
    • Hip screening
    • Cardiac assessment

Treatment Approach

  • Initial Management:
    • Early intervention crucial
    • Serial manipulation and casting
    • Dobbs method preferred
    • Weekly cast changes
  • Dobbs Method:
    • Reverse Ponseti technique:
      • Sequential hindfoot and forefoot correction
      • Pin fixation of talonavicular joint
      • Percutaneous Achilles tenotomy

Surgical Management

  • Limited Surgery:
    • Percutaneous talonavicular pinning
    • Achilles tenotomy
    • Anterior tibial tendon transfer
  • Extensive Surgery:
    • Single-stage correction:
      • Extensive soft tissue release
      • Talonavicular reduction
      • Pin fixation
      • Tendon balancing

Post-Treatment Care

  • Bracing Protocol:
    • Full-time bracing initially
    • Gradual weaning
    • Night bracing until age 4-5
  • Monitoring:
    • Regular radiographic assessment
    • Growth monitoring
    • Functional evaluation
    • Long-term follow-up

Complications and Outcomes

  • Potential Complications:
    • Recurrence (10-50%)
    • Overcorrection
    • Stiffness
    • Avascular necrosis
    • Wound problems
  • Long-term Outcomes:
    • Better with early treatment
    • Variable with associated conditions
    • Regular monitoring needed
    • Possible arthritis in adulthood


Further Reading
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