Clinical and Radiological Features Suggestive of Mucopolysaccharidosis in Two Siblings From Sudan: A Case Series
Alaa Bella1, Mumen Abdalazim Dafallah2, Ashraf Yousif Fadlalla1
1Internal Medicine Department University of Gezira Wad Madani Al Jazīrah Sudan.
Clinical Case Reports
|July 30, 2026
Abstract:
Mucopolysaccharidosis should be suspected in patients presenting with multisystem involvement, including coarse facial features, skeletal abnormalities, and progressive organ dysfunction, particularly in resource-limited settings where delayed diagnosis is common. Early clinical recognition is crucial, as timely diagnosis can facilitate appropriate supportive care, genetic counseling, ultimately improving quality of life.
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