MS is a rare and benign genetic disorder that requires a high index of suspicion for timely diagnosis. This unique case underscores the need for increased clinical awareness of MS in resource-limited settings where genetic testing is not common and the importance of multidisciplinary evaluation for accurate diagnosis and management. Timely diagnosis and treatment can prevent bone deformities, fractures, and disabilities and improve patient outcomes for this uncommon syndrome.
Faisal et al. (Thu,) studied this question.