Congenital lordosis
ICD-10 Q76.42 is a billable code used to indicate a diagnosis of congenital lordosis.
Congenital lordosis is a spinal deformity characterized by an excessive inward curvature of the lumbar spine, which can be present at birth or develop shortly thereafter. This condition may result from various factors, including genetic predispositions, intrauterine positioning, or associated congenital malformations. In pediatric patients, congenital lordosis can lead to significant functional limitations, discomfort, and potential complications such as nerve compression or altered gait patterns. Diagnosis typically involves clinical examination and imaging studies, such as X-rays or MRI, to assess the degree of curvature and rule out associated anomalies. Treatment options may vary from observation in mild cases to physical therapy, bracing, or surgical intervention in more severe instances. Early identification and management are crucial to optimize outcomes and prevent long-term complications associated with this condition.
Documentation should include detailed clinical findings, imaging results, and treatment plans. Growth and developmental assessments are also critical.
Pediatric patients presenting with back pain, abnormal gait, or developmental delays may require evaluation for congenital lordosis.
Consideration of family history and potential genetic syndromes associated with spinal deformities is essential for accurate coding.
Genetic testing results, family history, and any syndromic associations should be documented to support the diagnosis.
Patients with congenital lordosis may be evaluated for genetic syndromes such as Marfan syndrome or Ehlers-Danlos syndrome.
Understanding the genetic basis of associated conditions can aid in comprehensive coding and management.
Used in cases of severe congenital lordosis requiring surgical intervention.
Pre-operative assessments, imaging studies, and post-operative follow-up notes.
Orthopedic and pediatric surgical specialties should collaborate for comprehensive care.
Congenital lordosis is present at birth and may be associated with other congenital anomalies, while acquired lordosis develops later due to factors such as injury, obesity, or muscle imbalances. Accurate coding requires clear documentation of the condition's origin.
