ICD10 code of Pierre Robin Syndrome and ICD9 code

Pierre Robin Syndrome, also known as Robin sequence, is a rare congenital condition characterized by a combination of certain facial abnormalities. The condition is named after the French stomatologist Pierre Robin, who first described it in 1923. Individuals with Pierre Robin Syndrome typically present with a smaller than usual lower jaw (micrognathia), a tongue that falls back into the throat (glossoptosis), and a cleft palate.

In terms of medical coding, the International Classification of Diseases (ICD) provides codes to classify and identify specific medical conditions. For Pierre Robin Syndrome, the corresponding ICD10 code is Q87.0. This code falls under the category of "Congenital malformation syndromes predominantly affecting facial appearance" in the ICD10 coding system. It is important to note that ICD10 codes are alphanumeric and consist of a letter followed by two numbers.

In the previous ICD9 coding system, Pierre Robin Syndrome was classified under the code 756.0. This code was used to identify congenital anomalies of the face and jaw. However, it is worth mentioning that ICD9 codes are no longer in use as they have been replaced by the more comprehensive ICD10 coding system.

It is crucial to consult with a medical professional or healthcare provider for accurate diagnosis and coding of medical conditions. Proper coding allows for effective communication between healthcare providers, insurance companies, and researchers, facilitating appropriate medical care and reimbursement processes.

by Diseasemaps