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28 Julai 2026, 08:03:19
Physiological bowing and knocked knees
28 Julai 2026, 08:03:19
Physiological bowing (genu varum) and physiological knocked knees (genu valgum) are common developmental variations of lower limb alignment in children. These conditions are part of normal skeletal growth and usually resolve spontaneously without treatment. Physiological genu varum is most prominent from birth to approximately 18–24 months of age, after which the legs gradually straighten. Physiological genu valgum develops between 2 and 4 years of age, reaches a maximum around 3–4 years, and gradually corrects to the normal adult alignment by approximately 7–8 years of age.
Persistent, progressive, asymmetrical, or severe deformity may indicate an underlying pathological condition such as Blount disease, rickets, skeletal dysplasia, trauma, infection, or metabolic bone disease and requires further evaluation.
Pathophysiology
Lower limb alignment changes predictably during childhood as the skeleton matures. Infants are born with physiological genu varum due to intrauterine positioning. As weight bearing begins, remodelling of the proximal tibia and distal femur gradually corrects the bowing. Between 2 and 4 years of age, the mechanical axis shifts laterally, producing a temporary physiological genu valgum. Continued skeletal growth subsequently restores normal lower limb alignment.
Abnormal or persistent deformity occurs when normal growth plate development is disrupted. In Blount disease, excessive compressive forces across the medial proximal tibial physis suppress normal growth, resulting in progressive tibial varus deformity. In rickets, defective mineralization of growing bone weakens the growth plate, leading to progressive angular deformities under normal weight-bearing forces.
Normal developmental alignment
Age | Expected alignment |
Birth to 18 months | Physiological genu varum |
18–24 months | Neutral alignment |
2–4 years | Physiological genu valgum |
5–7 years | Gradual correction |
≥7 years | Adult alignment (approximately 5–7° valgus) |
Risk factors for pathological deformity
Obesity
Early walking
Vitamin D deficiency
Rickets
Blount disease
Skeletal dysplasia
Previous trauma
Previous physeal injury
Bone infection
Family history of skeletal disorders
Clinical presentation
Physiological deformity
Symmetrical bow legs or knock knees
Normal growth and development
Normal gait
No pain
No limp
No functional limitation
Normal height for age
Features suggesting pathological deformity
Progressive deformity
Asymmetrical deformity
Persistent genu varum beyond 2 years
Persistent genu valgum beyond 7 years
Intercondylar distance or intermalleolar distance greater than expected for age
Limb-length discrepancy
Pain
Limp
Short stature
Widened wrists or ankles
Features suggestive of rickets
Family history of skeletal dysplasia
Diagnostic approach
Diagnosis is primarily clinical and should distinguish physiological variants from pathological conditions.
Clinical examination
Assess:
Limb alignment
Gait
Symmetry
Intercondylar distance (genu varum)
Intermalleolar distance (genu valgum)
Knee range of motion
Limb-length discrepancy
Rotational profile
Height and growth pattern
Laboratory investigations (when pathology is suspected)
Serum calcium
Serum phosphate
Alkaline phosphatase
Serum 25-hydroxyvitamin D
Parathyroid hormone
Renal function tests
Imaging
Not routinely required for physiological deformity.
Indications include:
Persistent deformity outside the normal age range
Progressive deformity
Asymmetry
Suspicion of Blount disease
Suspicion of rickets
Limb-length discrepancy
Investigations:
Standing long-leg radiographs (preferred)
Plain knee radiographs
Bone age assessment when indicated
Differential diagnosis
Physiological genu varum
Physiological genu valgum
Blount disease
Nutritional rickets
Skeletal dysplasia
Osteogenesis imperfecta
Physeal injury
Bone tumours
Renal osteodystrophy
Non-pharmacological management
Physiological genu varum or genu valgum
Treatment is observation and parental reassurance.
Explain the normal pattern of lower limb development.
Routine activity restriction is unnecessary.
Encourage maintenance of a healthy body weight.
Encourage age-appropriate physical activity.
Review every 6 months until spontaneous correction occurs.
Braces, corrective shoes, wedges, and splints are not recommended for physiological deformities because they do not accelerate correction.
Pharmacological treatment
Routine drug therapy is not indicated in physiological bowing or physiological knocked knees.
If vitamin D deficiency or nutritional rickets is confirmed, treat according to current vitamin D deficiency or rickets guidelines.
Example:
Calcium 600 mg + Vitamin D 800 IU (PO) once daily for 3 months (adjust according to age and nutritional status).
Surgical management
Surgery is not indicated for physiological genu varum or genu valgum.
Children with persistent or pathological deformities should be referred to an orthopaedic surgeon.
Temporary hemiepiphysiodesis (guided growth)
Temporary hemiepiphysiodesis is the preferred treatment for skeletally immature children with significant angular deformity and adequate remaining growth.
Indications
Persistent genu valgum after approximately 7–8 years of age
Persistent genu varum after approximately 2–3 years when physiological causes have been excluded
Mechanical axis deviation causing functional impairment
Progressive deformity
Angular deformity generally exceeding 10–15°
Deformity secondary to Blount disease or skeletal dysplasia with remaining growth potential
Procedure
A tension-band plate ("eight-plate") or transphyseal screw is placed across one side of the growth plate.
Continued growth on the opposite side gradually corrects the deformity.
Clinical and radiographic review is recommended every 3–6 months.
The implant is removed once neutral mechanical alignment is achieved to avoid overcorrection.
Corrective osteotomy
Corrective osteotomy is indicated when:
Skeletal maturity has been reached.
The deformity is severe.
Guided growth is no longer possible.
Blount disease presents late with established deformity.
There is multiplanar deformity requiring immediate correction.
Common procedures include:
Proximal tibial valgus osteotomy for severe genu varum.
Distal femoral varus osteotomy for severe genu valgum.
Combined femoral and tibial osteotomy when deformity involves both bones.
Internal fixation with plates, screws, or external fixation may be used depending on the deformity and surgeon expertise.
Follow-up
Children should be reviewed every 6 months to assess:
Degree of deformity
Limb alignment
Growth
Gait
Functional status
Repeat standing radiographs are recommended only when progression or pathological deformity is suspected.
Prognosis
Physiological genu varum and genu valgum have an excellent prognosis. Most children achieve normal lower limb alignment without intervention. Early recognition of pathological causes such as Blount disease or rickets allows timely treatment and prevents permanent deformity, gait abnormalities, and early osteoarthritis.
