Marfan syndrome with aortic dilation
ICD-10 Q87.410 is a billable code used to indicate a diagnosis of marfan syndrome with aortic dilation.
Marfan syndrome is a genetic disorder affecting connective tissue, characterized by features such as tall stature, long limbs, and a predisposition to cardiovascular complications, particularly aortic dilation and dissection. Aortic dilation occurs when the aorta, the large artery that carries blood from the heart, becomes enlarged, which can lead to serious complications if not monitored and managed appropriately. Patients with Marfan syndrome often present with skeletal abnormalities, ocular issues, and cardiovascular problems. Early diagnosis and regular monitoring are crucial for managing the risk of aortic complications. Genetic testing can confirm the diagnosis, and echocardiograms are typically used to assess the aorta's size and function. Management may include lifestyle modifications, regular follow-ups, and surgical interventions if necessary. The condition is inherited in an autosomal dominant pattern, meaning that a single copy of the mutated gene from an affected parent can cause the disorder in offspring.
Pediatric documentation should include growth parameters, developmental milestones, and any associated congenital anomalies.
Common scenarios include routine check-ups for children diagnosed with Marfan syndrome, monitoring for aortic dilation, and referrals for orthopedic evaluations.
Pediatric coders should be aware of the growth patterns in children with Marfan syndrome and the implications for surgical interventions.
Genetic documentation must include family history, results of genetic testing, and any counseling provided to the family.
Scenarios include genetic counseling sessions for families with a history of Marfan syndrome and discussions about reproductive options.
Genetic coders should ensure that all genetic testing and counseling services are accurately documented and linked to the diagnosis.
Used for monitoring aortic dilation in patients with Marfan syndrome.
Documentation must include the indication for the echocardiogram and findings related to aortic dilation.
Pediatric cardiologists should ensure that the echocardiogram results are clearly linked to the diagnosis of Marfan syndrome.
Accurate coding of Marfan syndrome with aortic dilation is crucial for ensuring appropriate management and monitoring of cardiovascular risks associated with the condition. It also facilitates access to necessary genetic counseling and interventions.
