Limping in children is fairly common. The list of potential etiologies is long and varied and ranges from the benign to the life-threatening. [1, 2, 3] Patients most often present to their primary care physician or an emergency department for initial evaluation. An understanding of normal and abnormal gait is critical. 
Once a gait abnormality has been identified, a thorough history and physical examination should be undertaken to narrow the differential diagnosis. [5, 6] The history should focus on the characteristic of the pain itself, as well as the presence of systemic or constitutional symptoms. Physical examination can help localize the etiology. Patients often have tenderness or loss of range of motion at the site of pathology. Further laboratory and radiographic studies are obtained according to the findings from the history and physical examination.
Well-defined treatments exist for most causes and vary with the severity of the disease process or injury. Fortunately, most children respond well to therapy and resume walking normally without sequelae.
Various pathologies are responsible for limping in children. At times, differentiating normal developmental changes from disease states presents a difficult dilemma. Establishing a diagnosis can be quite challenging, and these patients often require assessment by more than one physician in more than one visit. Aggressively pursuing the source of a child’s limp at the first visit is essential to ensure optimal outcomes in the most patients.
Appropriate and early referral to an orthopedic specialist can benefit selected patients tremendously. However, in many instances, a conscientious physician can accurately assess and treat many of the conditions discussed in this article. Regardless, successful treatment of the child presenting with a limp demands sound clinical judgment, judicious ancillary testing, understanding of the possible differential diagnoses, and knowledge of therapeutic options.
For patient education resources, see Juvenile Rheumatoid Arthritis.
Normal synchronous gait develops in the first 3 years of life and requires the child to meet numerous anatomic and physiologic milestones. At age 1 year, many children can walk without support. By age 18 months, most children walk, and many can run. Coordination with reciprocal arm swing develops by age 2 years.
Appropriate gait is attained with adequate musculoskeletal development of the lower back, pelvis, and lower extremities. Normal neurologic growth is mandatory for coordination and balance. Myelinization in a cephalocaudal pattern may explain the lack of complete control over those muscles that are integral to adult gait.
Finer adjustments to the gait pattern may not occur until the child is aged 8-10 years, when normal adult gait pattern is attained. Adult gait patterns assume coordination of the following five key maneuvers:
However, for the purposes of this article, a more simplistic view of normal gait is described.
Normal gait begins with the stance phase, which is the weightbearing phase; it starts with the heel-strike. As the foot begins to plantarflex, the end of this phase culminates with the toe-off. The swing phase begins with toe-off and ends with the heel-strike. During the swing phase, coordinated gait requires forward rotation and tilting of the pelvis, as well as stability of the lumbar spine and abdomen. A limp or deviation from the normal expected walking pattern may be due to pain, weakness, or a structural abnormality.
Abnomalities of gait include the following:
A thorough history should be obtained from the child, if possible, and the parents. Parents’ input is integral to obtaining an accurate perception of the complaint. A limp may originate from disorders affecting the abdomen, genitourinary tract, back, pelvis, hip, knee, foot, or other areas of the body.
Specific characteristics of the pain should be queried. A mnemonic that may be helpful in this regard is OPQRST, defined as follows:
Additionally, the presence of systemic or constitutional symptoms is very important. The presence of fever, weight loss, night sweats, anorexia, or general malaise may indicate a more serious etiology. [7, 8, 9, 10, 11]
The child’s previous medical and surgical history should be ascertained, as well as recent travel, immunizations, sick contacts, and a history of the child’s development.
A complete physical examination is critical. The ultimate goals of the examination are to identify the type of limp (eg, antalgic, Trendelenburg, or spastic) and localize the site of pathology.
The physical examination should begin with an overall assessment of the child, including vital signs. Ideally, the child should be observed while barefoot and minimally clothed for assessment of stance and gait.
The child should be observed walking and running, if possible. Take the child into an open area to observe several gait cycles to elicit the gait abnormality and anatomic location. Running often accentuates subtle abnormalities. Range of motion of the individual joints should be observed. The specific type of nonantalgic gait should be identified, if possible. The differential of a child with a Trendelenburg gait may be different from that of the child with an equinus gait.
The abdomen, pelvis, back, and extremities of the supine or sitting child should be inspected and palpated. Inspection and palpation are best accomplished when the child is sitting comfortably in the mother’s lap. Areas of erythema, swelling, and warmth should be noted. Each digit and joint should be examined for motion and ligamentous stability.  Special attention should be given to the hips.
Neurovascular status, including strength, sensation, and reflexes, can also be assessed while the child is sitting or supine. Measure and compare lower-extremity lengths.
Laboratory assessment often begins with a complete blood count (CBC) and differential white blood cell (WBC) count, erythrocyte sedimentation rate (ESR), and possibly a C-reactive protein (CRP) level. [13, 14] These laboratory studies should be obtained when an infectious, inflammatory, or neoplastic etiology is suspected.
Common tests, such as electrolyte levels (eg, calcium), coagulation studies, and uric acid levels (to assess for gout), are occasionally necessary.
Sickle cell tests, Lyme disease titers, immunologic lab studies (eg, lupus antibodies, anti–double-stranded DNA, rheumatoid factor, human leukocyte antigen, creatine kinase) are occassionally indicated when a specific etiology is supected.
A study by Dubois-Ferrière et al found that in the initial workup of limping children with suspected transient synovitis of the hip, many of the common diagnostic tests are unnecessary; according to the authors, routine assessment need include only the WBC count, the CRP level, the ESR, and hip radiography and ultrasonography. 
In 2012, the American College of Radiology presented its biannual Appropriateness Criteria, consisting of evidence-based guidelines to rate the appropriateness of imaging and treatment procedures for specific clinical conditions. The guidelines were based on an analysis of the medical literature in peer-reviewed journals and the application of a well-established consensus methodology. 
Standard radiography is the initial imaging study of choice in the limping child. (See the images below.) Orthogonal images of the area of concern should be obtained. Because of the high incidence of referred pain, radiographs of the hips are routinely obtained. Orthogonal images of the hip should consist of anteroposterior and frog-leg lateral views, with the exception of a suspected slipped capital femoral epiphysis, in which case a frog-leg lateral position could lead to displacement and a true lateral should be obtained.
In very young children or those whose physical examination does not reveal a focal source of pain, radiographs of the entire lower extremity should be obtained. As many as 20% of children have unsuspected fractures. [17, 18]
A study from Scotland using a protocol that radiographically assessed only the affected anatomic site had good success diagnosing the cause of limp. 
Ultrasonography is also often used. [20, 21] It is effective in diagnosing a hip effusion; however, it is unable to differentiate a sterile from a purulent effusion. In the patient with a high concern for septic arthritis, ultrasonography can be useful for guiding aspiration.
Bone scintigraphy is frequently used when the history and physical examination and other imaging studies do not identify the source of injury or pathology. Bone scintigraphy with technetium-99m highlights areas of increased bone metabolism  and may help to identify occult fractures,  osteomyelitis,  stress fractures, tumor or metastatic disease, and Legg-Calvé-Perthes disease. 
One study found bone scanning to be a beneficial initial test after radiography for children aged 2-11 years who had no clear etiology for foot pain, whether bilateral or unilateral.  In a small group of patients (N=49), bone scans aided in both diagnosis and treatment for those children who had not received an advanced study such as computed tomography (CT) or magnetic resonance imaging (MRI). For some patients, obtaining a bone scan may be a good alternative when the diagnosis is not clear after history, physical examination, and plain radiography.
CT is effective for abdominal and pelvic pathology (eg, sacroiliac trauma) and bony pathology of the hip, knee, spine, and foot.
MRI is the study of choice for soft-tissue pathology. MRI is also very useful in diagnosing stress fractures, osteomyelitis, malignancy, and early Legg-Calvé-Perthes disease.
Synovial fluid analysis should include cell count and differential WBC count, glucose, culture and Gram stain, and crystal examination.
Mucin clot formation suggests a noninfectious etiology, as bacteria break down the normal hyaluronic acid found in synovial fluid.
Bone aspirates can be assessed with Gram stain and culture for identification of the bacteria that is causing the osteomyelitis.
Knowing the child’s age is imperative in diagnosing the cause of a limp. A brief summary of common disease states in different age groups is listed in Table 1 below.
Table 1. Common Causes of Limping in Children (Open Table in a new window)
Infectious or inflammatory
Synovitis – Viral, bacterial, atypical (Lyme disease)
Synovitis – Viral, bacterial, atypical (Lyme disease)
Most pathologic processes of the foot are nontraumatic in toddlers. Examining the children’s shoes and feet is imperative. Possible etiologies causing a limp include the following.
Microtrauma to the foot can result in stress fractures. Bone scans may be necessary for identification.
Ingrown toenails may cause limping. Standard incision and drainage and appropriate nail care are recommended.
Osteomyelitis may require both medical and surgical therapies, depending on the area of the foot involved and the extent of infection.  Subperiosteal abscess and failure to improve with medical management are indications for surgical treatment.
Puncture wounds can be managed conservatively with good local wound care and close follow-up. Patients who return with a wound infection or persistent pain should be evaluated for osteomyelitis, particularly that caused by Pseudomonas aeruginosa.
Toddler’s fracture, a spiral fracture of the distal one third of the tibia, is often stable and incomplete and may be the result of a trivial injury, which is often not witnessed.
Torus fractures resulting from impaction, spiral fractures resulting from torsional injury, and greenstick fractures resulting from direct trauma occur commonly in children. 
Physeal injuries are more commonly seen in the older child following a rotational injury.
The knee and patellofemoral joints are common sites of pain, particularly in the older child and adolescent.
Sports-related injuries and overuse syndromes as well as infection may affect the knee area.
A popliteal, or Baker, cyst may rupture. These cysts are found along the inferomedial aspect of the knee.
Osteochondritis dissecans represents separation of articular cartilage, usually of the distal femur from underlying bone.
Osgood-Schlatter disease, affecting the patellar tendon insertion into the tibial tubercle, usually occurs in adolescents.
Patellofemoral syndrome is often the result of tracking abnormalities of the patella or patellofemoral instability. Jumping, running, and climbing may all be affected as the articular surface of the patella becomes inflamed.
Knee effusions may be related to overuse, trauma, or systemic disease. Thorough history taking, laboratory screening, and arthrocentesis with appropriate referral are suggested. The differential diagnoses include juvenile arthritis, lupus erythematosus, and infectious arthritis (including Lyme disease). A knee effusion after injury, especially in the adolescent athlete, may signal ligamentous injury.
Lyme disease can present in a variety of ways; synovitis, pauciarticular arthritis, and polyarticular arthritis may occur.
Bloody effusions may be associated with trauma. Possible traumatic causes include distal femur and proximal tibia fractures, tibial spine avulsions, patella fractures, and, rarely, knee dislocations.
Trauma, metabolic diseases, neoplasia, congenital deformities, and infection affect the thigh and femur.
Pathologic fractures related to tumors (benign or malignant), metabolic bone disease, or child abuse should be suspected with femoral shaft fractures. A fracture through a unicameral bone cyst in the proximal femur is not uncommon.
Metaphyseal beak fractures and rotational injuries that cause spiral deformities suggest possible child abuse.
Contusions of the thigh musculature are common in patients of all ages but may occasionally be debilitating and serious.
The distal femoral physis grows faster than any other physis in the body. According to Phemister’s law, malignant and benign bone tumors occur in regions of the most rapid growth. Malignant tumors, including osteogenic sarcoma and Ewing sarcoma, generally produce more cortical destruction and periosteal reaction on radiographs than do benign lesions.
Osteomyelitis is usually due to hematogenous seeding, but it may also be the result of direct inoculation. Pain and swelling at the distal femur may represent osteomyelitis. In half of cases, the causative organism is Staphylococcus aureus. No organism is identified in as many as one quarter of cases. Examine radiographs of the affected bone for abnormalities within the soft-tissue planes, cortical destruction, and periosteal elevation or thickening. Magnetic resonance imaging (MRI) or technetium-99m bone scanning may assist in localization.
Developmental dysplasia of the hip is thought to be due, in part, to laxity of the hip joint capsule, prenatal and postnatal position, and genetic and environmental factors.  When recognized and treated early, most dislocatable hips stabilize in the first 4-6 weeks of life and develop without sequelae. On occasion, the femoral head remains dislocated, thereby precluding normal development.
Useful physical examination tests include the Ortolani maneuver, Barlow test, and Galeazzi sign. Ultrasonography or plain radiography may confirm the findings. Patients with late or undiagnosed dysplasia often present with a waddling gait or a painful limp.
In children, trauma to the hip is more likely to result in a dislocation than a fracture. Prompt reduction of the dislocated hip usually results in few complications.
Hip fractures in children are associated with numerous complications, including avascular necrosis, premature closure of the epiphyseal plate, coxa vara, and nonunion.
Older children may experience avulsion of muscular attachments to the pelvis or proximal femur. Avulsion of the iliopsoas from the lesser trochanter or disruption from the ischial apophysis can occur (especially after sporting-event injuries).
Differentiating between transient synovitis and septic arthritis of the hip can be challenging. Both present with the leg held in flexion, abduction, and external rotation, representing the position of largest capsular volume. Clinically, most children with septic arthritis are toxic and present with fever, anorexia, and joint pain. Features of septic arthritis include hematogenous spread and purulent effusion. Articular destruction is due to proteolytic enzymes, most commonly S aureus. The hip, knee, and ankle are most commonly affected.
Ultrasonography of the hip has been shown to be effective to assess for osteomyelitis, septic arthritis, transient synovitis, Legg-Calvé-Perthes disease, and developmental dysplasia of the hip. [33, 34, 35, 36, 37]
Kocher et al proposed a clinical prediction algorithm to help differentiate between transient synovitis and septic arthritis of the hip.  The probability of septic arthritis was predicted on the basis of the following four factors:
This algorithm has not been prospectively tested. Kocher et al recommended diagnostic arthrocentesis in patients with two to four positive factors and close observation for patients with no predictors. Patients with only one positive variable had a 5% or less chance of having septic arthritis.
An elevated C-reactive protein (CRP) level has been shown to be a good indicator of septic arthritis and should be included as part of the evaluation.
On synovial fluid analysis, a WBC count higher than 50,000/μL with a predominance of polymorphonuclear (PMN) cells favors a diagnosis of septic arthritis, which is a surgical emergency.  Transient synovitis is generally associated with lower counts and fewer PMN cells. Gram stain and culture help guide antibiotic therapy.
Legg-Calvé-Perthes disease typically affects boys in the first decade. AVN of the capital femoral epiphysis results in remodeling of the femoral head and acetabulum over 1-3 years. Flattening of the femoral head may be a late finding. Acute presentations are associated with synovitis of the hip. [40, 41]
Slipped capital femoral epiphysis usually affects large-for-age adolescents.  It presents with a limp associated with hip pain or referred pain to the thigh or knee.  Delayed diagnosis is not uncommon, because of referred symptoms. Most cases are unilateral, but bilateral involvement is possible.  The second slip often presents 6-18 months later.
Anteroposterior pelvic radiographs may reveal subtle widening of the physis, though the frog-leg lateral projection may be more helpful at identifying subtle slips. A Klein line, drawn along the superior femoral neck, may intersect less or none of the femoral head on the affected side.
Hip pathology often presents with thigh or knee pain.
Infection, rheumatologic disease, microtrauma, and neoplasia of the spine, pelvis, or abdomen may result in a limp. In general, these disease processes are more common in the older child or adolescent.
Juvenile ankylosing spondylitis and rheumatoid arthritis may cause back pain.
Neoplastic diseases affecting the pelvis, spine, and abdomen include neuroblastoma, leukemia, osteogenic sarcoma, and renal tumors.
Overuse syndromes are common in active adolescents.
Spondylolysis due to a stress fracture of the pars interarticularis is found most commonly at L5.
Herniated nucleus pulposus in the older child or adolescent presents in a similar fashion as in adults but is much less common.
Diskitis, inflammation of the intervertebral disk, may be infectious or, less likely, may be sterile. MRI may be necessary to identify the pathology.
Abdominopelvic lesions, which manifest solely as a limp, are uncommon. Such pathology often involves the retroperitoneum and includes appendicitis, psoas abscess, retroperitoneal hematoma, and renal/ureteral inflammation.
Pelvic entities include osteomyelitis, genitourinary infections, and tumors or hernias.
Skin and lymphatic diseases in the inguinal region may cause pain, swelling, and a limp.
Herman MJ, Martinek M. The limping child. Pediatr Rev. 2015 May. 36 (5):184-95; quiz 196-7. [Medline].
Wyndham M. The limping child. Community Pract. 2007 Sep. 80(9):42. [Medline].
Abbassian A. The limping child: a clinical approach to diagnosis. Br J Hosp Med (Lond). 2007 May. 68(5):246-50. [Medline].
Sutherland DH, Olshen R, Cooper L, Woo SL. The development of mature gait. J Bone Joint Surg Am. 1980 Apr. 62(3):336-53. [Medline].
Gekeler J. Radiology of adolescent slipped capital femoral epiphysis: measurement of epiphyseal angles and diagnosis. Oper Orthop Traumatol. 2007 Oct. 19(4):329-44. [Medline].
Ahmad WS, Lind T. [Discoid lateral meniscus as the cause of limping in children]. Ugeskr Laeger. 2008 Oct 13. 170(42):3339. [Medline].
Sinigaglia R, Gigante C, Bisinella G, Varotto S, Zanesco L, Turra S. Musculoskeletal manifestations in pediatric acute leukemia. J Pediatr Orthop. 2008 Jan-Feb. 28(1):20-8. [Medline].
Sonnen GM, Henry NK. Pediatric bone and joint infections. Diagnosis and antimicrobial management. Pediatr Clin North Am. 1996 Aug. 43(4):933-47. [Medline].
McCanny PJ, McCoy S, Grant T, Walsh S, O’Sullivan R. Implementation of an evidence based guideline reduces blood tests and length of stay for the limping child in a paediatric emergency department. Emerg Med J. 2013 Jan. 30(1):19-23. [Medline].
Swischuk LE. The limping infant: imaging and clinical evaluation of trauma. Emerg Radiol. 2007 Sep. 14(4):219-26. [Medline].
Unkila-Kallio L, Kallio MJ, Eskola J, Peltola H. Serum C-reactive protein, erythrocyte sedimentation rate, and white blood cell count in acute hematogenous osteomyelitis of children. Pediatrics. 1994 Jan. 93(1):59-62. [Medline].
Unkila-Kallio L, Kallio MJ, Peltola H. The usefulness of C-reactive protein levels in the identification of concurrent septic arthritis in children who have acute hematogenous osteomyelitis. A comparison with the usefulness of the erythrocyte sedimentation rate and the white blood-cell count. J Bone Joint Surg Am. 1994 Jun. 76(6):848-53. [Medline].
Dubois-Ferrière V, Belaieff W, Lascombes P, de Coulon G, Ceroni D. Transient synovitis of the hip: which investigations are truly useful?. Swiss Med Wkly. 2015. 145:w14176. [Medline].
Milla SS, Coley BD, Karmazyn B, Dempsey-Robertson ME, Dillman JR, Dory CE, et al. ACR Appropriateness Criteria® limping child–ages 0 to 5 years. J Am Coll Radiol. 2012 Aug. 9 (8):545-53. [Medline].
Walter KD, Tassone JC. Orthopedics. Marcdante KJ, Kliegman RM, eds. Nelson Essentials of Pediatrics. 7th ed. Philadelphia: Saunders; 2014. 667.
Renshaw TS. The child who has a limp. Pediatr Rev. 1995 Dec. 16(12):458-65. [Medline].
Abernethy LJ, Lee YC, Cole WG. Ultrasound localization of subperiosteal abscesses in children with late-acute osteomyelitis. J Pediatr Orthop. 1993 Nov-Dec. 13(6):766-8. [Medline].
Perez RH, Alonso Farto JC, Arias IA, Regi AR, Perez Vazquez JM. Small rounded B-cell lymphoma of bone presented by limp, with a positive multifocal 99mTc MDP bone scintigraphy pattern and a negative 99mTc HMPAO-labeled leukocytes study. J Pediatr Hematol Oncol. 2008 Jun. 30(6):443-6. [Medline].
Oudjhane K, Newman B, Oh KS, et al. Occult fractures in preschool children. J Trauma. 1988 Jun. 28(6):858-60. [Medline].
Chudnofsky CR, Sebastian S. Special wounds. Nail bed, plantar puncture, and cartilage. Emerg Med Clin North Am. 1992 Nov. 10(4):801-22. [Medline].
[Legg-Calvé-Perthes disease–diagnostics and contemporary treatment]. Srp Arh Celok Lek. 2008 Jul-Aug. 136(7-8):430-4. [Medline].
Hazany SJ, Bader SR, Hazany D, Ly NT, Otsuka NY. Use of radioisotope bone scans in children with obscure foot pain. J Pediatr Orthop B. 2011 Jul. 20(4):252-6. [Medline].
Morrissy RT, Shore SL. Bone and joint sepsis. Pediatr Clin North Am. 1986 Dec. 33(6):1551-64. [Medline].
Kunnamo I, Kallio P, Pelkonen P, Hovi T. Clinical signs and laboratory tests in the differential diagnosis of arthritis in children. Am J Dis Child. 1987 Jan. 141(1):34-40. [Medline].
Khoury J, Jerushalmi J, Loberant N, Shtarker H, Militianu D, Keidar Z. Kohler disease: diagnoses and assessment by bone scintigraphy. Clin Nucl Med. 2007 Mar. 32(3):179-81. [Medline].
Weber-Chrysochoou C, Corti N, Goetschel P, Altermatt S, Huisman TA, Berger C. Pelvic osteomyelitis: a diagnostic challenge in children. J Pediatr Surg. 2007 Mar. 42(3):553-7. [Medline].
Alpert SW, Ben-Yishay A, Koval KJ, Zuckerman JD, eds. Fractures and Dislocations: A Manual of Orthopaedic Trauma. New York: Lippincott-Raven; 1994. 152-93.
Aronsson DD, Goldberg MJ, Kling TF Jr, Roy DR. Developmental dysplasia of the hip. Pediatrics. 1994 Aug. 94(2 Pt 1):201-8. [Medline].
Howard CB, Eihoran M, Dagan R, Nyska M. The use of ultrasound in children with pain around the hip and thigh. Isr J Med Sci. 1993 Feb-Mar. 29(2-3):77-81. [Medline].
Terjesen T. Ultrasonography in the primary evaluation of patients with Perthes disease. J Pediatr Orthop. 1993 Jul-Aug. 13(4):437-43. [Medline].
Wenger DR. Slipped capital femoral epiphysis. Wenger DR, Rang M, eds. The Art and Practice of Children’s Orthopaedics. New York: Raven Press; 1993. 331-71.
Causey AL, Smith ER, Donaldson JJ, et al. Missed slipped capital femoral epiphysis: illustrative cases and a review. J Emerg Med. 1995 Mar-Apr. 13(2):175-89. [Medline].
Kocher MS, Zurakowski D, Kasser JR. Differentiating between septic arthritis and transient synovitis of the hip in children: an evidence-based clinical prediction algorithm. J Bone Joint Surg Am. 1999 Dec. 81(12):1662-70. [Medline].
Welkon CJ, Long SS, Fisher MC, Alburger PD. Pyogenic arthritis in infants and children: a review of 95 cases. Pediatr Infect Dis. 1986 Nov-Dec. 5(6):669-76. [Medline].
Chiarapattanakom P, Thanacharoenpanich S, Pakpianpairoj C, Liupolvanish P. The remodeling of the neck-shaft angle after proximal femoral varus osteotomy for the treatment of Legg-Calve-Perthes syndrome. J Med Assoc Thai. 2012 Oct. 95 Suppl 10:S135-41. [Medline].
Pfeifer R, Zelle BA, Kobbe P, Knobe M, Garrison RL, Ohm S, et al. Impact of isolated acetabular and lower extremity fractures on long-term outcome. J Trauma Acute Care Surg. 2012 Feb. 72(2):467-72. [Medline].
Infectious or inflammatory
Synovitis – Viral, bacterial, atypical (Lyme disease)
Synovitis – Viral, bacterial, atypical (Lyme disease)
Jeremy K Rush, MD Pediatric Orthopaedic Surgeon, San Antonio Military Medical Center, Fort Sam Houston, TX
Jeremy K Rush, MD is a member of the following medical societies: American Academy of Orthopaedic Surgeons, Pediatric Orthopaedic Society of North America, Pediatric and Adolescent Sports Medicine Research Society
Disclosure: Nothing to disclose.
Francisco Talavera, PharmD, PhD Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference
Disclosure: Received salary from Medscape for employment. for: Medscape.
George H Thompson, MD Director of Pediatric Orthopedic Surgery, Rainbow Babies and Children’s Hospital, University Hospitals Case Medical Center, and MetroHealth Medical Center; Professor of Orthopedic Surgery and Pediatrics, Case Western Reserve University School of Medicine
George H Thompson, MD is a member of the following medical societies: American Orthopaedic Association, Scoliosis Research Society, Pediatric Orthopaedic Society of North America, American Academy of Orthopaedic Surgeons
Disclosure: Received none from OrthoPediatrics for consulting; Received salary from Journal of Pediatric Orthopaedics for management position; Received none from SpineForm for consulting; Received none from SICOT for board membership.
Jeffrey D Thomson, MD Professor of Orthopedic Surgery, University of Connecticut School of Medicine; Director of Orthopedic Surgery, Connecticut Children’s Medical Center; Vice President of Medical Staff, Connecticut Children’s Medical Center
Disclosure: Nothing to disclose.
Charles T Mehlman, DO, MPH Professor of Pediatrics and Pediatric Orthopedic Surgery, Division of Pediatric Orthopedic Surgery, Director, Musculoskeletal Outcomes Research, Cincinnati Children’s Hospital Medical Center
Charles T Mehlman, DO, MPH is a member of the following medical societies: American Academy of Pediatrics, American Fracture Association, Scoliosis Research Society, Pediatric Orthopaedic Society of North America, American Medical Association, American Orthopaedic Foot and Ankle Society, American Osteopathic Association, Arthroscopy Association of North America, North American Spine Society, Ohio State Medical Association
Disclosure: Nothing to disclose.
Christopher B Beach, MD, FACEP, FAAEM Associate Professor and Vice Chairman of Emergency Medicine, Department of Emergency Medicine, Northwestern University, The Feinberg School of Medicine
Christopher B Beach, MD, FACEP, FAAEM is a member of the following medical societies: Alpha Omega Alpha, American Academy of Emergency Medicine, American College of Emergency Physicians, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose. James R Ficke, MD Assistant Professor of Surgery, Uniformed Services University of Health Sciences F Edward Hebert School of Medicine; Clinical Instructor, Department of Physical Therapy, Baylor University; Orthopedic Consultant, US Army Surgeon General, Chairman, Department of Orthopedics and Rehabilitation, Brooke Army Medical Center
James R Ficke, MD is a member of the following medical societies: American Academy of Orthopaedic Surgeons, American Orthopaedic Association, American Orthopaedic Foot and Ankle Society, Orthopaedic Trauma Association, and Society of Military Orthopaedic Surgeons
Disclosure: Nothing to disclose.
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