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A congenital anal septum is a condition characterized by the presence of an abnormal wall or membrane that separates the anus into two distinct cavities, rather than allowing for the normal single tubular canal. This condition is typically present at birth and can lead to complications if not addressed. In the procedure associated with CPT® Code 46070, the anal septum in an infant is surgically divided. The process begins with a thorough inspection of the anus to assess the extent of the septum. Once the evaluation is complete, the septum is sharply incised, effectively creating a single tubular anal canal. This surgical intervention is crucial for restoring normal anatomy and function, thereby alleviating potential issues related to bowel movements and overall gastrointestinal health in the affected infant.
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