Limited diagnostic facilities impending the therapeutic approach of Mucopolysaccharidosis in Bangladesh: A case report [post]

Orindom Shing Pulock, Susmita Dey Pinky, Syeda Humaida Hasan
2022 unpublished
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.
doi:10.22541/au.164386096.61334829/v1 fatcat:r5e6uylfbfcgzedjommwcifxia