Amber Wiggins-McDaniel

Diagnosis and Current Treatment Strategies for Adult and Juvenile Hereditary Hemochromatosis

Tori Tyler, Amber Wiggins-McDaniel, Staton McBroom, Caroline Parry, Robert Tyler & Robert A. White · Biotechnology Journal International · 2024

Hemochromatosis is a common genetic disorder manifesting as an iron overload state requiring complex processes in diagnosis, treatment, and management of both adult, and pediatric, populations. This review outlines general diagnostic and treatment strategies for hemochromatosis d...

Open access Research Article 10.9734/bji/2024/v28i2718

A Comprehensive Review of Duchenne Muscular Dystrophy: Genetics, Clinical Presentation, Diagnosis, and Treatment

Kylie A. Limback, William D. Jacobus, Amber Wiggins-McDaniel, Ramon Newman & Robert A. White · Biotechnology Journal International · 2022

Duchenne Muscular Dystrophy (DMD) is a genetic disorder involving progressive muscle deterioration leading to loss of mobility, cardiomyopathy, and respiratory complications leading to an early death by the fourth decade of life. Males are affected more often as DMD results from...

Open access Research Article 10.9734/bji/2022/v26i6662