Coronal craniosynostosis
ICD-10 Q75.02 is a billable code used to indicate a diagnosis of coronal craniosynostosis.
Coronal craniosynostosis is a congenital condition characterized by the premature fusion of the coronal suture, which runs from ear to ear across the top of the skull. This early closure restricts the growth of the skull perpendicular to the suture, leading to a characteristic head shape that may appear flattened on one side (plagiocephaly) and bulging on the forehead. The condition can result in increased intracranial pressure, developmental delays, and facial asymmetry. Diagnosis is typically made through physical examination and imaging studies such as CT scans. Treatment often involves surgical intervention to correct the skull shape and allow for normal brain growth. Early diagnosis and management are crucial to prevent complications and support optimal neurodevelopment in affected infants.
Detailed growth and developmental assessments, family history, and physical examination findings.
Infants presenting with abnormal head shape, developmental delays, or increased intracranial pressure.
Consideration of the timing of diagnosis and intervention, as well as the need for ongoing developmental assessments.
Genetic testing results, family pedigree, and any syndromic associations.
Cases where craniosynostosis is part of a genetic syndrome requiring genetic counseling.
Understanding the implications of genetic syndromes on treatment and prognosis.
Used in surgical correction of coronal craniosynostosis.
Operative report detailing the procedure and indications.
Neurosurgery documentation standards.
Documenting associated syndromes is crucial as it impacts treatment decisions, prognosis, and the need for multidisciplinary care. Accurate coding ensures appropriate reimbursement and reflects the complexity of the patient's condition.
