Lambdoid craniosynostosis, unspecified
ICD-10 Q75.049 is a billable code used to indicate a diagnosis of lambdoid craniosynostosis, unspecified.
Lambdoid craniosynostosis is a congenital condition characterized by the premature fusion of the lambdoid suture, which is located at the back of the skull. This fusion restricts the growth of the skull in the affected area, leading to an abnormal head shape, often described as a flattening on one side of the head. The condition can result in increased intracranial pressure, developmental delays, and potential neurological issues if not addressed. Diagnosis typically involves a physical examination and imaging studies such as CT scans to assess the skull shape and suture fusion. Treatment often requires surgical intervention to correct the skull shape and allow for normal brain growth. The condition may occur as an isolated anomaly or as part of a syndrome, necessitating a thorough evaluation for associated congenital malformations or chromosomal abnormalities.
Pediatric documentation should include growth parameters, developmental milestones, and any associated conditions.
Common scenarios include infants presenting with abnormal head shape during routine check-ups or referrals for developmental delays.
Considerations include the age of the child, potential for neurodevelopmental impact, and the timing of surgical intervention.
Genetic documentation should include family history, genetic testing results, and any syndromic associations.
Scenarios may involve genetic counseling for families with a history of craniosynostosis or related syndromes.
Considerations include the need for genetic evaluation to rule out syndromic causes and the implications for family planning.
Used in surgical correction of lambdoid craniosynostosis.
Surgical reports detailing the procedure and indications.
Pediatric surgical documentation must include pre-operative assessments and post-operative follow-up.
Lambdoid craniosynostosis is a congenital condition where the lambdoid suture fuses prematurely, leading to an abnormal head shape and potential complications such as increased intracranial pressure and developmental delays.
