Congenital absence of both lower leg and foot, left lower limb
ICD-10 Q72.22 is a billable code used to indicate a diagnosis of congenital absence of both lower leg and foot, left lower limb.
Congenital absence of both the lower leg and foot on the left side is a significant limb reduction defect that occurs during fetal development. This condition can arise from various factors, including genetic predispositions, environmental influences, or teratogenic exposures. Clinically, it presents as the complete absence of the left lower leg and foot, which can impact mobility and overall development in pediatric patients. Children with this condition may require multidisciplinary care, including orthopedic evaluation, prosthetic fitting, and physical therapy to enhance functional outcomes. The absence of the limb can also be associated with other congenital anomalies, necessitating a thorough evaluation for associated conditions. Early intervention is crucial to optimize developmental milestones and improve quality of life.
Documentation should include detailed clinical findings, family history, and any associated congenital anomalies. Growth and developmental assessments are also critical.
Common scenarios include initial diagnosis at birth, follow-up visits for growth and development, and assessments for prosthetic needs.
Consideration for developmental milestones and the psychosocial impact of limb absence on the child and family.
Genetic evaluation may include family history, genetic testing results, and assessment for syndromic associations.
Scenarios may involve genetic counseling for families with a history of congenital limb defects or syndromes associated with limb reduction.
Understanding the genetic basis of limb reduction defects and their potential inheritance patterns is crucial for accurate coding.
Used for surgical interventions related to limb absence or reconstruction.
Detailed operative notes and justification for the procedure.
Orthopedic specialists should provide comprehensive documentation to support the procedure.
Documentation should include a clear diagnosis of the congenital absence, details of any associated anomalies, and a comprehensive clinical history to support the coding decision.
