II. Precautions
- See Limping Child for acute painful gait
- This Pediatric Leg Disorder topic addresses the more chronic, progressive pediatric leg abnormalities
III. History
- Distinguish between 2 types of Gait Abnormality (critical first step)- Acute, Antalgic Gait (painful) resulting in Limping Child (urgent evaluation)- See Limping Child
 
- Chronic, progressive, nonantalgic gait or other leg abnormality (non-Traumatic)- Described here
 
 
- Acute, Antalgic Gait (painful) resulting in Limping Child (urgent evaluation)
- Past medical history and growth and development- Prenatal and birth history
- Breech Delivery (Congenital Hip Dysplasia, Femoral Anteversion)
- Developmental Milestones
- Medical history (Trauma, surgery or hospitalizations)
- Dietary intake (adequate Calcium, Vitamin D)
 
- History of Present Illness- Timing- Age of onset and duration
- Progression
 
- Associated findings (red flags)- Pain with activity and limiting play
- Limping, tripping or falling
 
 
- Timing
IV. Exam: Systemic Signs
- Growth- Height and weight with growth percentiles and Body Mass Index
- Normal growth decreases likelihood of underlying systemic condition (e.g. Rickets, metabolic bone disease)
 
- Facial Appearance- Abnormal facies may suggest genetic disorder (e.g. fragile X)
 
- Neurologic- See Developmental Delay
- See Muscle Weakness in Children
- Neuromuscular disorders
- Cerebral Palsy
- Muscular Dystrophy
 
- Skin- Ecchymosis
- Midline spinal skin changes (e.g. dermal sinus, midline Lipoma, sacral dimple)
- Neurocutaneous Syndrome (e.g. Cafe-Au-Lait Macule)
- Inflammation (redness, warmth, swelling)- Infection (e.g. Septic Arthritis)
- Rheumatologic Disorders
 
 
V. Exam: Gait
- See Gait Evaluation in Children
- Distinguish between painful (antalgic) and non-painful (nonantalgic) Abnormal Gait
- 
                          Antalgic Gait
                          - Stance phase on unaffected limb is shortened due to pain
- Refusal to bear weight especially with limited range of motion, systemic symptoms, fever
 
- Nonantalgic gait
VI. Exam: General Musculoskeletal
- 
                          General- Expose the extremities (in shorts, underwear, diaper)
- Evaluate for symmetry
- Evaluate for Leg Length Discrepancy (>2 cm difference is significant)
 
- Joint Inflammation (Joint Swelling, warmth, and painful range of motion)- Inflammatory Arthritis
- Septic Arthritis (non-weight bearing)
- Reactive Arthritis
 
- 
                          Muscle
                          - Muscular atrophy: Disuse atrophy or neurologic disorder
- Calf hypertrophy: Muscular Dystrophy
 
- 
                          Joint Laxity
                          - Associated angular deformities (e.g. Genu Varum, Genu Valgum)
- Congenital Hip Dysplasia
- Connective Tissue Disorders
 
- Bone Tenderness- Fracture or bone Contusion
- Bone Tumor (may present with palpable bone mass)
- Osteomyelitis
 
- Spine- Evaluate spinal flexion and extension
- Evaluate for Scoliosis, lumbar lordosis, thoracic kyphosis
 
VII. Exam: Hip and Pelvis
- See Hip Exam
- See Hip Rotation Evaluation in Children
- See Hip Range of Motion
- Gluteal or thigh skin fold asymmetry
- Galeazzi Sign (one knee higher than the other)
- 
                          FABER Test or Pelvic Compression Test positive- Sacroiliac Joint Disorder
 
- 
                          Trandelenburg Test positive- Congenital Hip Dysplasia
- Weak hip adductors
- Leg Length Discrepancy
 
- 
                          W-Sitting Position
                          - Associated with Femoral Anteversion (but NOT a cause of Femoral Anteversion)
- Patient sits on floor with each heel adjacent to the ipsilateral hip- Hips flexed and externally rotated
- Knees maximally flexed
 
 
- Hip resting position flexed and externally rotated- Slipped Capital Femoral Epiphysis- Hip unable to be abducted or internally rotated
 
- Hip Joint effusion- Hip abducted
 
 
- Slipped Capital Femoral Epiphysis
- Hip internal rotation lost- Aseptic Necrosis of the Femoral Head
- Slipped Capital Femoral Epiphysis
- Intraarticular hip disorder
 
- Limited hip abduction- Congenital Hip Dysplasia (positive Ortolani Maneuver or Barlow Test)
 
- Pelvic compression resulting in pain- Sacroiliac joint disorder
- Pelvis Trauma
 
VIII. Exam: Leg
- 
                          Foot Deformity- See Pediatric Foot Evaluation
- See Gait Evaluation in Children
- See Foot Anatomy
- Consider common foot disorders- Clubfoot (tiptoe walking, fixed equinus position)
- Metatarsus Adductus (foot cause of In-Toeing)
- Calcaneovalgus Deformity (Out-toeing)
- Pes Planus (flat arch while standing)
 
 
- Rotational Deformity
- Angular Deformity- Nearly all newborns start with Genu Varum- Neutral position by age 2 years
- Genu Valgum by age 3-6 years
- Returns to neutral or slightly valgus position (esp girls), by age 7-11 years old
 
- Evaluate standing knee alignment- Intercondylar distance
- Intermalleolar distance
- Tibiofemoral angle
 
- Risk Factors- Osteogenesis Imperfecta
- Rickets
- Renal Osteodystrophy
- Skeletal Dysplasia
- Klinefelter Syndrome
- Rheumatologic Disorders (Genu Valgum-like deformity)
 
- Disorders- Genu Varum (bow leg)
- Genu Valgum (knock knee)
 
 
- Nearly all newborns start with Genu Varum
IX. Differential Diagnosis
- Acute, Antalgic Gait (painful) resulting in Limping Child- See Causes of Limp in Children
- See Leg Pain
- See Foot Pain
 
- Chronic, progressive, nonantalgic gait or other leg abnormality- See Gait Evaluation in Children
- See Abnormal Gait in Children
- Intoeing- See In-Toeing
- Metatatarsus adductus (onset age <1 year)
- Internal Tibial Torsion (onset age 1 to 3 years)
- Femoral Anteversion (onset age 3 to 6 years, usually bilateral)
 
- Out-toeing- See Out-toeing
- Femoral Retroversion (resolves by age 1-2 years)
- Pes Planus (resolves by age 10 years)
- External Tibial Torsion (onset age 4-7 years)
 
- Genu Varum (Bowed Legs)- See Genu Varum
- Typically resolves in normal development by age <2 years
- Rickets
- Skeletal dysplasia
- Blount's disease (Obesity)
- Tibial Bowing- Anterolateral bowing (Neurofibromatosis association)
- Posteromedial bowing (In utero calcaneovalgus foot, will spontaneously correct)
 
- Load-bearing, high-impact sports (teens)
 
- Genu Valgum (Knock-Knee)- See Genu Valgum
- Typical onset by age 1 to 3 years and resolves in normal development by age 8 years
- Rickets
- Diastrophic dysplasia
- Morquio's Syndrome
- Ellis-van Creveld or Chondroectodermal Dysplasia
- Spondyloepiphyseal Dysplasia
- Pseudoachondroplasia
 
 
