The ICD-10 code for Wyburn-Mason Syndrome is Q28.2. This code is used to classify this rare congenital disorder characterized by arteriovenous malformations in the brain, retina, and face. Unfortunately, there is no specific ICD-9 code for this syndrome as it was replaced by ICD-10 in 2015. It is important to consult with a healthcare professional for accurate diagnosis and coding.
Wyburn-Mason Syndrome, also known as Wyburn-Mason arteriovenous malformation syndrome, is a rare congenital disorder characterized by the presence of arteriovenous malformations (AVMs) in various parts of the body. These AVMs can affect different organs such as the brain, retina, face, and oral cavity. However, it's important to note that ICD-10 codes are not assigned to specific syndromes, but rather to individual diseases or conditions.
For the AVMs associated with Wyburn-Mason Syndrome, the appropriate ICD-10 codes would depend on the specific location and manifestation of the malformations. For example, if the AVMs primarily affect the retina, the ICD-10 code H35.059 (Retinal arteriovenous malformation) could be applicable. If the AVMs involve other organs, additional codes may be required to accurately capture the condition.
It's worth mentioning that the International Classification of Diseases, 10th Revision (ICD-10) replaced the 9th Revision (ICD-9) in 2015. Consequently, there is no specific ICD-9 code for Wyburn-Mason Syndrome. However, in ICD-9, codes such as 747.81 (Arteriovenous malformation, acquired) or 759.6 (Arteriovenous malformation) might have been used to describe the presence of AVMs in various locations.
Remember, it's always important to consult with a healthcare professional for an accurate diagnosis and appropriate coding based on the specific manifestations and locations of the AVMs associated with Wyburn-Mason Syndrome.