The landscape of rare genetic disorders has been revolutionized by advances in understanding and treating Mucopolysaccharidosis (MPS) conditions. These inherited lysosomal storage diseases affect thousands of individuals worldwide, presenting complex clinical challenges that require specialized expertise and multidisciplinary care approaches. The accumulation of glycosaminoglycans in...

Sturge-Weber Syndrome emerges as a particularly challenging neurocutaneous condition that profoundly impacts patients, families, and healthcare providers across diverse medical settings. This congenital disorder, distinguished by characteristic facial port-wine birthmarks, complex neurological manifestations, and serious ocular complications such as glaucoma, presents unique diagnostic and...