Longitudinal reduction defect of left fibula
ICD-10 Q72.62 is a billable code used to indicate a diagnosis of longitudinal reduction defect of left fibula.
Longitudinal reduction defect of the left fibula is a congenital malformation characterized by the underdevelopment or absence of the fibula bone on the left side. This condition can lead to significant functional impairments, including limb length discrepancies, gait abnormalities, and potential complications in the development of the foot and ankle. The fibula plays a crucial role in stabilizing the ankle and supporting the muscles of the lower leg. In cases of longitudinal reduction defects, the affected limb may exhibit a range of deformities, including clubfoot or other structural abnormalities. Diagnosis typically involves imaging studies such as X-rays or MRI to assess the extent of the defect and any associated anomalies. Management may include orthopedic interventions, physical therapy, and in some cases, surgical correction to improve function and alignment. Early intervention is essential to optimize outcomes and support the child's mobility and overall development.
Detailed growth and developmental assessments, including physical examination findings and functional limitations.
A pediatric patient presenting with a limb length discrepancy and gait abnormalities requiring orthopedic evaluation.
Consideration of the child's age and developmental milestones when planning interventions.
Genetic testing results, family history of congenital conditions, and any syndromic associations.
A child with a longitudinal reduction defect undergoing genetic counseling for potential syndromic associations.
Awareness of chromosomal abnormalities that may co-occur with limb reduction defects.
Used in cases where surgical intervention is required to correct alignment.
Pre-operative assessments, imaging studies, and surgical notes.
Orthopedic specialists should ensure comprehensive documentation of the defect and surgical rationale.
Accurate coding of Q72.62 is crucial for appropriate reimbursement, tracking of congenital conditions, and ensuring that patients receive the necessary multidisciplinary care. It also aids in research and understanding the prevalence and outcomes of such congenital defects.
