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Limited diagnostic facilities impending the therapeutic approach of Mucopolysaccharidosis in Bangladesh: A case report
  • Orindom Shing Pulock,
  • Susmita Dey Pinky,
  • Syeda Humaida Hasan
Orindom Shing Pulock
Chattogram Medical College and Hospital

Corresponding Author:mrospulock@gmail.com

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Susmita Dey Pinky
Chattogram Medical College and Hospital
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Syeda Humaida Hasan
Chattogram Medical College and Hospital
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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.
23 Jan 2022Submitted to Clinical Case Reports
25 Jan 2022Assigned to Editor
25 Jan 2022Submission Checks Completed
03 Feb 2022Reviewer(s) Assigned
13 Apr 2022Review(s) Completed, Editorial Evaluation Pending
15 Apr 2022Editorial Decision: Revise Minor