Limited diagnostic facilities impending the therapeutic approach of
Mucopolysaccharidosis in Bangladesh: A case report
In resource-constrained settings, mucopolysaccharidosis (MPS) is a rare
hereditary metabolic illness that frequently remains undiagnosed. We
present a scenario that illustrates the challenges in diagnosing and
managing MPS due to test inaccessibility, as well as potential
approaches to minimize the hurdles.