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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


Disclaimer

The notes provided on Pediatime are generated from online resources and AI sources and have been carefully checked for accuracy. However, these notes are not intended to replace standard textbooks. They are designed to serve as a quick review and revision tool for medical students and professionals, and to aid in theory exam preparation. For comprehensive learning, please refer to recommended textbooks and guidelines.





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