Other reduction defects of right lower limb
ICD-10 Q72.891 is a billable code used to indicate a diagnosis of other reduction defects of right lower limb.
Q72.891 refers to congenital malformations characterized by the partial or complete absence of one or more structures in the right lower limb. These defects can arise from genetic factors, environmental influences, or a combination of both during fetal development. Commonly associated conditions include limb reduction defects, which may manifest as phocomelia (absence of limbs), amelia (absence of a limb), or other variations in limb length and structure. The right lower limb may exhibit abnormalities in bones, muscles, and soft tissues, leading to functional impairments. Diagnosis typically involves physical examination, imaging studies, and genetic testing to identify any underlying chromosomal abnormalities. Management may include orthopedic interventions, physical therapy, and, in some cases, surgical procedures to improve function and appearance. Early intervention is crucial for optimizing developmental outcomes in affected children.
Detailed clinical notes on the child's developmental milestones, physical examination findings, and any interventions performed.
A pediatric patient presenting with a clubfoot and limb reduction defect requiring orthopedic evaluation and treatment.
Ensure accurate coding of associated conditions, such as scoliosis or hip dysplasia, which may coexist.
Genetic testing results, family history of congenital conditions, and any syndromic associations.
A child with a limb reduction defect undergoing genetic counseling to assess for chromosomal abnormalities.
Consider the implications of genetic syndromes that may present with limb defects, requiring careful coding.
Used in cases where limb reduction defects require surgical intervention.
Document the indication for surgery and any preoperative assessments.
Orthopedic specialists should ensure accurate coding based on the surgical procedure performed.
Comprehensive documentation should include a detailed clinical description of the limb defect, any associated congenital anomalies, results from imaging studies, and genetic testing if applicable. Ensure that the specific limb affected is clearly identified.
