International Journal of Obstetric Anesthesia
Volume 17, Issue 2 , Pages 170-173 , April 2008

Anaesthetic management of an obstetric patient with Pompe disease

,Accepted 1 November 2007.

References 

  1. Kishnani PS, Steiner RD, Bali D, et al. Pompe disease diagnosis and management guideline. Genet Med. 2006;8:267–288
  2. Genzyme Corporation. A Physician’s Guide to Pompe Disease. www.pompe.com (accessed 7/11/2007).
  3. Raben N, Plotz P, Byrne BJ. Acid α-glucosidase deficiency (Glycogenosis Type II, Pompe disease). Curr Mol Med. 2002;2:145–166
  4. Hirschhorn R, Reuser AJJ. Glycogen storage disease type II: acid alpha-glucosidase (acid maltase) deficiency. In:  Scriver CR, et al. editor. The Metabolic and Molecular Bases of Inherited Disease. 8th ed.. New York: McGraw-Hill; 2001;p. 3389–3420
  5. Pollard BJ, Harrison MJ. Anaesthesia for Uncommon Diseases. Carlton: Blackwell Scientific; 1989;95–96
  6. Mason R. Anaesthesia Databook. A Perioperative and Peripartum Manual. 3rd ed. Greenwich Medical Media, 2001: 405–7.
  7. Vercauteren M. Obstetric spinal analgesia and anesthesia. Curr Opin Anaesthesiol. 2003;16:503–507

PII: S0959-289X(07)00181-1

doi: 10.1016/j.ijoa.2007.11.001

International Journal of Obstetric Anesthesia
Volume 17, Issue 2 , Pages 170-173 , April 2008

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