Course Outline
Click on the links below to preview selected pages from this course.
- What are Prions?
- Theories Regarding Prion Infection
- Research
- Theories
- Hypothesis
- Multi-component Hypothesis
- Symptoms and Histopathology of Prion Disease
- Infectious Prion Diseases
- Other Human Prion Diseases
- Laboratory Safety
- Diagnosis
- References
Additional Information
Level of Instruction: Intermediate
Intended Audience: Medical laboratory scientists, medical laboratory technicians, histotechnologists, and histotechnicians working in the clinical or pathology laboratory. This course is also appropriate for medical laboratory science students, histology students, and pathology residents.
Author Information:
Garland E. Pendergraph, PhD, JD, MLS(ASCP)SM, HCLD/CC(ABB) received his MSPH from the University of Kentucky in Lexington, his PhD in medical parasitology/entomology and mycology from the University of North Carolina in Chapel Hill, and his law degree with a concentration in health care law from Concord Law School, Purdue University. He also did a Fellowship in Tropical Medicine at Louisiana State University School of Medicine. He is the author of a textbook on phlebotomy, a number of scientific articles, plus internet training programs. He is the director of five laboratories.
Kwi Simmons is employed as a Clinical Coordinator at Piedmont Macon Hospital. She is certified as a MLS (ASCP) receiving her BS degree in medical technology from Thomas University and her Master of Science degree in clinical molecular genetics from Northern Michigan University.
Reviewer Information: Judi Bennett is a program director for MediaLab, Inc. During her 30 year career as a medical technologist, she has served as a senior system analyst, laboratory manager, Point-of-Care coordinator, microbiology supervisor, and generalist. Judi has been a speaker at various LIS, AMT, and CLMA conferences and has been published in CLMA magazine.
Course Description: This course includes an overview of the function of prion proteins and the differing theories as to how prions cause several different neurodegenerative diseases. The causes and symptoms of the four types of infectious and classical prion diseases will be explored, as well as the recommendations for safe handling of blood and body fluid specimens from individuals infected with prion diseases.
