Journal of Obesity and Metabolism
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Yong Hung
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Gaucher Disease Complications: A Case of Gaucheroma and Protein-Losing Enteropathy
Gaucher disease, a genetic lysosomal storage disorder, is characterized by the accumulation of glucocerebrosides due to a deficiency in the enzyme glucocerebrosidase. This case report highlights a patient diagnosed with Gaucher disease who developed rare complications: gaucheroma and protein-losing enteropathy. The patient presented with abdominal ... Read More»
: J Obes Metab 2024, 7:241
10.4172/jomb.1000241Abstract Peer-reviewed Full Article Peer-reviewed Article PDF Mobile Full Article
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