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This case report explores management strategies for Gaucher Disease Type 1 in a child, highlighting the lack of enzyme replacement therapy.
This case report depicts the management of an 8‐year‐old male with Gaucher Disease Type 1, manifesting as massive splenomegaly, anemia, and skeletal involvement in a resource‐constrained environment. Treated with splenectomy due to the absence of enzyme replacement therapy, it underscores the necessity for enhanced therapeutic access and comprehensive care.
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Shah et al. (2025) studied this question.
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