Longitudinal reduction defect of femur, bilateral
ICD-10 Q72.43 is a billable code used to indicate a diagnosis of longitudinal reduction defect of femur, bilateral.
Longitudinal reduction defect of the femur is a congenital malformation characterized by the underdevelopment or absence of the femur bone in one or both legs. In bilateral cases, both femurs are affected, leading to significant implications for mobility and overall limb function. This condition can result from genetic factors, environmental influences, or a combination of both. Clinically, patients may present with shortened limbs, abnormal gait, and associated deformities such as hip dysplasia or scoliosis. Diagnosis typically involves imaging studies, including X-rays or MRI, to assess the extent of the defect and any associated musculoskeletal anomalies. Management may include orthopedic interventions, physical therapy, and in some cases, surgical procedures to improve limb function and alignment. Early intervention is crucial for optimizing developmental outcomes in affected children.
Detailed growth and developmental assessments, including physical examinations and treatment plans.
A pediatric patient presenting with bilateral femur reduction defects requiring orthopedic evaluation and intervention.
Consideration of developmental milestones and the impact of the defect on mobility and daily activities.
Genetic testing results, family history, and any syndromic associations.
Referral for genetic counseling in cases of suspected syndromic congenital limb defects.
Understanding the genetic basis of limb reduction defects and their potential hereditary implications.
Used in surgical correction of femur defects.
Surgical notes detailing the procedure and indications.
Orthopedic documentation must include pre-operative assessments.
Documenting associated conditions is crucial as it provides a comprehensive view of the patient's health status, informs treatment planning, and ensures accurate coding for reimbursement.
