Congenital shortening of unspecified lower limb
ICD-10 Q72.819 is a billable code used to indicate a diagnosis of congenital shortening of unspecified lower limb.
Congenital shortening of the lower limb is a condition characterized by the underdevelopment or reduction in length of one or both lower limbs, which can occur due to various congenital malformations or deformations. This condition may arise from genetic factors, environmental influences, or a combination of both. It can manifest as part of broader syndromes or as an isolated anomaly. Congenital shortening can lead to functional impairments, affecting mobility and overall quality of life. Associated conditions may include limb reduction defects, clubfoot, and hip dysplasia, which can complicate the clinical picture. Diagnosis typically involves physical examination, imaging studies, and sometimes genetic testing to identify underlying chromosomal abnormalities. Treatment may include orthopedic interventions, physical therapy, and in some cases, surgical procedures to improve limb function and alignment. Early intervention is crucial for optimizing outcomes in affected children.
Detailed growth and development assessments, including physical examination findings and any associated conditions.
A pediatric patient presenting with unilateral limb shortening and associated clubfoot requiring orthopedic evaluation.
Consideration of developmental milestones and the impact of limb shortening on mobility and function.
Genetic testing results, family history of congenital anomalies, and any syndromic associations.
A child with congenital shortening of the lower limb undergoing genetic counseling for potential syndromic causes.
Understanding the genetic basis of limb malformations and the implications for family planning.
Used in cases of significant limb shortening requiring surgical intervention.
Pre-operative assessments, imaging studies, and surgical notes.
Orthopedic evaluation and planning are essential for surgical candidates.
Documentation should include a detailed clinical assessment, imaging results, any associated congenital conditions, and treatment plans to support the diagnosis.
