Marden-Walker syndrome, also known as MWS, is a rare genetic disorder characterized by multiple physical and developmental abnormalities. Unfortunately, I am unable to provide you with the specific ICD-10 code for MWS as it is not within my current capabilities. However, I can offer you some general information about the condition.
Marden-Walker syndrome is typically associated with distinctive facial features, such as a flat or sunken midface, hypertelorism (widely spaced eyes), and a small jaw. Individuals with MWS may also present with joint contractures, clubfoot, and a significant delay in motor and cognitive development. Additionally, they may have respiratory issues, feeding difficulties, and visual impairments.
As for the ICD-9 code, the transition from ICD-9 to ICD-10 occurred in 2015, making ICD-9 codes outdated. However, the previous ICD-9 code used for Marden-Walker syndrome was 759.89, which encompassed "other specified congenital anomalies."
It is crucial to consult with a healthcare professional or medical coding specialist to obtain the most accurate and up-to-date information regarding the specific ICD-10 code for Marden-Walker syndrome.