Glycogen Storage Disease IXc with PHKG2 Mutation and Psoriatic-Like Lesions: A Rare Case
Glycogen storage diseases (GSDs) cause glycogen metabolism disorders in the human body and are genetically determined metabolic illnesses. Due to sufficient glycogen or its diseased states, glycogen is accumulated in the human body tissues due to the enzymatic defect during glycogenolysis/glycogen...
محفوظ في:
| المؤلفون الرئيسيون: | , , , , , , |
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| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
Liaquat National Hospital and Medical College
2025-08-01
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| سلاسل: | Journal of Liaquat National Hospital |
| الموضوعات: | |
| الوصول للمادة أونلاين: | https://journals.lnh.edu.pk/jlnh/pdf/ec55bab5-8b85-4d85-89d9-c83a439d9202.pdf |
| الوسوم: |
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