Resulting Condition: Paroxysmal Nocturnal Hemoglobinuria
Über den Vortrag
Der Vortrag „Resulting Condition: Paroxysmal Nocturnal Hemoglobinuria“ von Richard Mitchell, MD, PhD ist Bestandteil des Kurses „NCM 112 Care of Clients with Problems in Oxygenation, Fluid and Electrolytes, Inflammatory and Immunologic Response, and Cellular Aberrations (Philippines Nursing Curriculum)“.
Quiz zum Vortrag
Which of the following is involved in the pathophysiology of paroxysmal nocturnal hemoglobinuria?
- Loss of complement inhibitory proteins
- Loss of function mutation on chromosome 8
- A defect in the genes of the membrane protein spectrin
- Impairment of protoporphyrin synthesis
- Deficiency of vitamins that are necessary for hematopoiesis
Patients with paroxysmal nocturnal hemoglobinuria are at increased risk for which of the following disorders?
- Myelodysplastic syndrome
- Acute splenic sequestration crisis
- Subacute combined degeneration of the spinal cord
- Atopic dermatitis (eczema)
- Burkitt lymphoma
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Dozent des Vortrages Resulting Condition: Paroxysmal Nocturnal Hemoglobinuria
Richard Mitchell, MD, PhD
Dr. Richard N. Mitchell is the Lawrence J. Henderson Professor of Pathology and Health Sciences and Technology, at Harvard Medical School in Massachusetts, USA.
He obtained his PhD in Cell Biology and Immunology from Rockefeller University in 1980, and his MD from Harvard Medical School in 1984. Currently, he is Program Director of the Health Sciences and Technology Education and Curriculum at Harvard Medical School.
Due to his achievements, he earned the ASIP Robbins Distinguished Educator Award in 2013.
Within Lecturio, Dr. Mitchell teaches courses on Pathology.
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