Craniofacial dysostosis
ICD-10 Q75.1 is a billable code used to indicate a diagnosis of craniofacial dysostosis.
Craniofacial dysostosis, also known as craniosynostosis, is a congenital condition characterized by the premature fusion of one or more cranial sutures, leading to abnormal head shape and facial features. This condition can result in increased intracranial pressure, developmental delays, and various associated anomalies. The severity and specific manifestations depend on which sutures are involved and the timing of the fusion. Commonly associated features include ocular abnormalities, hearing loss, and dental issues. Treatment often involves surgical intervention to correct the skull shape and alleviate pressure on the brain. Early diagnosis and management are crucial for optimal outcomes, particularly in pediatric patients, as they are still undergoing significant growth and development.
Detailed growth and developmental assessments, imaging studies, and surgical reports.
Diagnosis of craniosynostosis in infants presenting with abnormal head shape, referral for surgical evaluation.
Consideration of developmental milestones and potential neurodevelopmental assessments.
Genetic testing results, family history of congenital conditions, and syndromic associations.
Genetic counseling for families with a history of craniofacial dysostosis or related syndromes.
Understanding the genetic basis of syndromic forms of craniosynostosis and implications for family planning.
Used in surgical correction of craniosynostosis.
Surgical reports detailing the procedure and indications.
Neurosurgery and pediatric surgery documentation standards.
Craniofacial dysostosis refers to a group of congenital conditions characterized by the abnormal fusion of cranial sutures, leading to altered skull shape and potential neurological complications.
