Anesthetic Management “Arnold Chiari Malformation” in the well-known Case of Cystic Fibrosis
International Clinical Neuroscience Journal,
Vol. 7 No. 4 (2020),
28 September 2020
,
Page 216-218
Abstract
Cystic fibrosis (CF) is a genetic disease resulting from a chlorine channel defect with autosomal recessive show, a physical and functional disorder in the transport of chlorine (Cl) through the plasma membrane in epithelial cells in organs such as the lungs, pancreas, liver, intestines, sweat glands, and epididymis. These cases are important for their perioperative respiratory complications. We present an anesthesia method conducted on a 24-year-old men CF case receiving general anesthesia for Arnold Chiari malformation surgery.
- Anesthesia
- Cystic Fibrosis
- Arnold Chiari malformation (ACM)
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References
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