Spondyloarthritis (SpA) comprises a spectrum of chronic inflammatory conditions that share common clinical features, laboratory abnormalities, and imaging features, and genetically tend to be associated with human leukocyte antigen B27 (HLA-B27). 1 The spectrum includes radiographic axial SpA (axSpA, known as ankylosing spondylitis [AS]), nonradiographic axSpA (nr-axSpA), psoriatic arthritis, inflammatory bowel disease-related arthritis, reactive arthritis, and undifferentiated SpA. 1,2 The onset of symptoms tends to occur at a relatively young age, often when patients are in their 20s. 1 The reported age at the time of initial symptom presentation in North Africa and the Middle East, including Saudi Arabia, Qatar, United Arab Emirates, Kuwait, and Egypt ranges between 23 and 32 years. 3-7 AxSpA primarily involves the sacroiliac joints and/or spine. 1 Establishing a diagnosis of axSpA, particularly at an early stage in the disease, can be challenging. 8 In 2009, the Assessment