Congenital absence of unspecified foot and toe(s)
ICD-10 Q72.30 is a billable code used to indicate a diagnosis of congenital absence of unspecified foot and toe(s).
Congenital absence of unspecified foot and toe(s) refers to a condition where one or both feet and/or toes are absent at birth. This condition can result from various developmental anomalies during gestation, leading to limb reduction defects. The absence may be complete or partial and can affect the functionality of the limb. Congenital absence of the foot and toes can be associated with other congenital malformations, such as clubfoot, where the foot is twisted out of shape or position, or hip dysplasia, which affects the hip joint's formation. These conditions may require multidisciplinary management, including orthopedic intervention, physical therapy, and possibly surgical correction. Accurate coding is essential for appropriate treatment planning and resource allocation in pediatric care, as these conditions can significantly impact a child's mobility and quality of life.
Detailed pediatric history and physical examination findings, including the extent of limb involvement and associated conditions.
A newborn presenting with absent toes during a routine examination or a child with a history of limb reduction defects requiring orthopedic evaluation.
Consideration of developmental milestones and the impact of the absence on mobility and daily activities.
Genetic testing results, family history of congenital anomalies, and any syndromic associations.
Referral for genetic counseling in cases of congenital limb anomalies with suspected hereditary patterns.
Understanding the genetic basis of congenital malformations and the implications for family planning.
Used in cases where surgical intervention is required for congenital absence.
Detailed operative report and pre-operative assessment.
Orthopedic evaluation and planning for prosthetic fitting.
Documentation should include a detailed clinical examination, imaging studies if performed, and any associated congenital anomalies. It is essential to specify the extent of the absence and any functional implications.
