Topic of Choice
The paper will discuss Wolman’s Disease
Reason for Choice
Wolman Disease is a unique disease that is common in Infants. Its infection and risk factors called for the need to research about it. Therefore, the need to research on its causes, diagnosis and care for the patients.
Disease Overview
Wolman disease is a lysosomal storage disease caused by a deficiency in lysosomal acid lipase, a condition development of mutations in the lysosomal lipase acid (LIPA) gene. The enzyme is a critical one, especially in the infant bodies, as it is responsible for the degradation of cholesterol in the lysosome. The pamphlet will provide a detailed overview of Wolman disease concerning its signs and symptoms, risks contributing to its onset, diagnosis and preventive steps, therapies, and outcomes from the affected patients. The review pamphlet will also discuss the current and future research demands on the treatment, diagnosis, and curve for Wolman disease.
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Pamphlet Format
Introduction to Wolman Disease
Symptoms and Signs of Wolman Disease
Risk factors associated with the disease and its prevention
Diagnosis and therapeutic
Outcomes of Wolman Disease
Future Research on treatment, Diagnosis and curve
Conclusion
Resources to be used.
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Sun, A., Chang, I. J., Lam, C., & Berry, G. T. Lysosomal Storage Disorders. In Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics (pp. 563-682). Content Repository Only!.
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