Congenital absence of hand and finger
ICD-10 Q71.3 is a billable code used to indicate a diagnosis of congenital absence of hand and finger.
Congenital absence of hand and finger refers to a condition where one or more fingers or the entire hand is absent at birth. This condition can occur as an isolated anomaly or as part of a syndrome involving other congenital malformations. The absence can result from genetic factors, environmental influences during pregnancy, or a combination of both. It is essential to assess the extent of the absence, as it can significantly impact the child's functional abilities and development. Associated conditions may include limb reduction defects, which can affect the musculoskeletal system, leading to challenges in mobility and dexterity. Early intervention, including physical therapy and occupational therapy, is crucial for optimizing the child's functional outcomes. Genetic counseling may also be indicated, especially if the absence is part of a broader syndrome or if there is a family history of congenital anomalies. Accurate coding is vital for appropriate management and resource allocation in pediatric care.
Detailed clinical notes describing the extent of absence, functional assessments, and any associated conditions.
A pediatric patient presenting with congenital absence of fingers requiring occupational therapy for adaptive skills.
Consideration of developmental milestones and the need for multidisciplinary care.
Genetic testing results, family history, and any syndromic associations must be documented.
A child with congenital absence of hand referred for genetic counseling due to family history of limb anomalies.
Understanding the genetic basis of congenital anomalies and implications for family planning.
Used for rehabilitation of a child with congenital absence of hand.
Document the specific exercises and goals for therapy.
Pediatric occupational therapy may require additional documentation for insurance purposes.
Documentation should include a detailed description of the congenital absence, any associated anomalies, family history, and the clinical management plan. This ensures accurate coding and appropriate reimbursement.
