Hypertelorism
ICD-10 Q75.2 is a billable code used to indicate a diagnosis of hypertelorism.
Hypertelorism is a congenital condition characterized by an increased distance between the orbits (eye sockets), which can be a feature of various syndromes and genetic disorders. This condition can lead to aesthetic concerns and may be associated with other congenital malformations, particularly those affecting the musculoskeletal system. Hypertelorism can occur as an isolated finding or as part of a syndrome, such as Crouzon syndrome or Apert syndrome, where it may be accompanied by craniosynostosis, limb deformities, or other anomalies. The condition is typically diagnosed through clinical examination and imaging studies, such as CT scans, which can help assess the degree of orbital separation and any associated craniofacial abnormalities. Management may involve multidisciplinary care, including surgical intervention for cosmetic and functional improvement, particularly if associated with other structural anomalies. Early diagnosis and intervention are crucial for optimizing outcomes in affected children.
Detailed clinical notes describing the extent of hypertelorism and any associated musculoskeletal anomalies.
Pediatric patients presenting with hypertelorism alongside clubfoot or limb reduction defects.
Ensure accurate coding of any associated congenital malformations to reflect the full clinical picture.
Genetic testing results and family history that may indicate syndromic associations.
Genetic counseling sessions for families with a history of congenital anomalies, including hypertelorism.
Consider the implications of genetic syndromes that may include hypertelorism and their associated coding.
Surgical intervention for cosmetic correction of hypertelorism.
Pre-operative assessment and surgical notes detailing the procedure.
Ophthalmology and plastic surgery may be involved in the management.
Accurate coding of hypertelorism is crucial for proper reimbursement, tracking of congenital anomalies, and ensuring that patients receive appropriate multidisciplinary care. It also aids in research and understanding of associated syndromes.
