Congenital absence of left foot and toe(s)
ICD-10 Q72.32 is a billable code used to indicate a diagnosis of congenital absence of left foot and toe(s).
Congenital absence of the left foot and toe(s) is a rare congenital malformation characterized by the complete or partial absence of the left foot and associated toes. This condition can occur as an isolated anomaly or as part of a syndrome involving other congenital defects. The absence may result from genetic factors, environmental influences during pregnancy, or a combination of both. Clinically, it is essential to assess the extent of the limb deficiency, as it can significantly impact mobility and function. Children with this condition may require orthopedic interventions, prosthetic fitting, and physical therapy to enhance their mobility and quality of life. Early diagnosis and management are crucial for optimal outcomes, and multidisciplinary care involving pediatricians, orthopedic surgeons, and rehabilitation specialists is often necessary. The condition may also be associated with other musculoskeletal anomalies, such as clubfoot or limb reduction defects, necessitating comprehensive evaluation and management.
Detailed clinical notes describing the child's developmental milestones, physical examination findings, and any interventions performed.
Assessment of a newborn with limb deficiency, follow-up visits for prosthetic fitting, and physical therapy evaluations.
Consideration of growth and development in children with limb deficiencies, as well as the psychosocial impact on the child and family.
Genetic testing results, family history of congenital anomalies, and any syndromic associations.
Genetic counseling for families with a history of congenital limb deficiencies and evaluation for syndromic conditions.
Understanding the genetic basis of congenital malformations and the implications for family planning and recurrence risk.
Used for surgical interventions related to limb deficiencies.
Detailed operative notes and justification for the procedure.
Orthopedic surgeons should provide comprehensive documentation to support the necessity of the procedure.
Documentation should include a clear diagnosis of congenital absence, details of any associated anomalies, and treatment plans. Clinical notes should specify the extent of the absence and any interventions performed.
