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BS Nursing Pathophysiology
nmdcat.online June 6, 2026

A patient with a genetic mutation develops cystic fibrosis. The primary defect in cystic fibrosis involves:

A. Impaired hemoglobin synthesis.
B. Abnormal chloride transport across cell membranes.
✓
C. Autoimmune destruction of pancreatic cells.
D. Defective muscle protein.

📖 Additional Information

  • Impaired hemoglobin synthesis.
  • Abnormal chloride transport across cell membranes.
  • Autoimmune destruction of pancreatic cells.
  • Defective muscle protein.

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