Metopic craniosynostosis
ICD-10 Q75.03 is a billable code used to indicate a diagnosis of metopic craniosynostosis.
Metopic craniosynostosis is a congenital condition characterized by the premature fusion of the metopic suture, which runs from the top of the head down the forehead. This early closure can lead to a triangular-shaped forehead and a narrow skull, affecting the overall head shape and potentially leading to increased intracranial pressure and developmental delays. The condition is often associated with other craniofacial anomalies and may require surgical intervention to correct the skull shape and allow for normal brain growth. Diagnosis is typically made through physical examination and imaging studies, such as CT scans, which can confirm the suture fusion. Treatment options include surgery to correct the skull shape and alleviate any associated complications. Early diagnosis and intervention are crucial for optimal outcomes in affected infants.
Detailed growth and development assessments, imaging results, and surgical notes.
Infants presenting with abnormal head shape, referrals for craniofacial evaluation, and pre- and post-operative assessments.
Ensure comprehensive documentation of developmental milestones and any associated syndromic features.
Family history, genetic testing results, and syndromic evaluations.
Genetic counseling for families with a history of craniosynostosis or related syndromes.
Consideration of genetic syndromes that may present with craniosynostosis, requiring thorough documentation of genetic evaluations.
Used for surgical correction of metopic craniosynostosis.
Operative report detailing the procedure and indications.
Pediatric surgical documentation must include pre-operative assessments and post-operative follow-up.
The primary treatment for metopic craniosynostosis is surgical intervention, typically performed in the first year of life to correct the skull shape and prevent complications associated with increased intracranial pressure.
