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Pes planus

Last updated: June 12, 2024

Summarytoggle arrow icon

Pes planus (flatfoot) is a type of foot deformity characterized by the absence or reduction of the medial longitudinal arch while standing. Pes planus can be rigid or functional. In rigid pes planus, the arch is absent regardless of foot position, while in functional pes planus, the medial arch is visible when sitting or standing on tiptoes. Rigid pes planus is rare and may be congenital or acquired. Functional pes planus is the most common type and is typically a painless, normal physiological variant that resolves by adolescence. Functional pes planus is typically diagnosed clinically and rarely requires further evaluation. Referral to an orthopedic surgeon should be considered for patients with pain or limited function.

This article covers functional pes planus; see “Subtypes and variants” for rigid pes planus and acquired pes planus.

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Epidemiologytoggle arrow icon

  • Occurs in > 95% of children ≤ 2 years of age [1]
  • Prevalence decreases with age: seen in < 20% of adults [1][2]

Epidemiological data refers to the US, unless otherwise specified.

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Etiologytoggle arrow icon

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Clinical featurestoggle arrow icon

Symptoms

Examination

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Subtypes and variantstoggle arrow icon

Rigid pes planus [2]

  • Definition: a form of pes planus where the medial arch remains flattened, regardless of foot positioning
  • Etiology
    • Congenital
    • Acquired
      • Trauma
      • Infection
      • Arthritis
      • Neuromuscular disease
  • Diagnostics
  • Treatment
    • Treat the underlying cause.
    • Further management depends on symptoms and can include orthotics and surgery.

Congenital rigid pes planus [3]

  • Definition: rare, complex foot deformity with a fixed vertical position of the talus and luxation of the talocalcaneonavicular joint
  • Etiology
    • Can be inherited in an autosomal dominant pattern [3]
    • Associated with neurological and/or genetic disorders
  • Pathogenesis
  • Clinical features
  • Diagnostics [3]
    • Foot examination
      • Head of the talus: palpable to touch
      • Medial longitudinal arch: stiff and flat with standing and sitting; no change with tiptoe standing [2]
    • Comprehensive neurological examination to rule out comorbid conditions [3]
    • X-ray foot: Axes of the tibia and talus appear parallel on the lateral image.
  • Treatment: Refer to an orthopedic surgeon for management. [2][3]
    • Serial casting of the newborn's limb: to restore anatomical foot alignment to optimize weight distribution
    • Surgery (e.g., open reduction): often performed before 3 years of age in patients with abnormal bony fusion (e.g., tarsal coalition) [2]

Acquired pes planus [4]

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Diagnosistoggle arrow icon

General principles [1]

Do not perform routine imaging to diagnose asymptomatic functional pes planus. [5]

Confirmatory examination findings [1][2]

  • “Too many toes” sign
    • Observe the patient from behind while they stand or walk.
    • Characteristic finding: Toes in addition to the fifth and half of the fourth toe are seen.
  • Medial arch position: can help differentiate between rigid and functional pes planus
    • Functional pes planus
      • Medial arch disappears when standing
      • Medial arch becomes visible again with dorsiflexion of the great toe while standing (also known as the “toe raising test”) or with tiptoe standing
      • In mild deformity, the arch may be visible on standing; standing on one foot may reveal arch collapse.
    • Rigid pes planus: the medial arch does not change with position

Assessment for underlying etiology [1][2]

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Treatmenttoggle arrow icon

Custom orthotics or shoe inserts are not recommended for patients with asymptomatic, or minimally symptomatic, pes planus. [6]

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Complicationstoggle arrow icon

We list the most important complications. The selection is not exhaustive.

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