Pregnancy during enzyme replacement therapy for late-onset acid maltase deficiency

Neuromuscul Disord. 2013 Feb;23(2):180-1. doi: 10.1016/j.nmd.2012.11.006. Epub 2013 Jan 3.

Abstract

We report the case of a female patient who developed Pompe's disease when she was 19. She received enzyme replacement therapy from the age of 35, and after three years of treatment the improvement in her clinical condition was such that she was able to consider having a baby. It was the patient's wishes to continue with her treatment throughout the entirety of her pregnancy. There were no complications, but there was a clear deterioration in motor and respiratory functions. She delivered at term by Caesarean section, and the child was healthy. Six months later, we noted an improvement of her motor and respiratory functions. The child was developing normally.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Age of Onset
  • Enzyme Replacement Therapy* / adverse effects
  • Female
  • Glycogen Storage Disease Type II / drug therapy*
  • Glycogen Storage Disease Type II / epidemiology
  • Glycogen Storage Disease Type II / physiopathology
  • Humans
  • Motor Activity / drug effects
  • Motor Activity / physiology
  • Pregnancy / physiology*
  • Pregnancy Complications / epidemiology
  • Pregnancy Outcome
  • Respiratory System / drug effects
  • Respiratory System / physiopathology
  • Risk Factors
  • alpha-Glucosidases / pharmacology
  • alpha-Glucosidases / therapeutic use*

Substances

  • alpha-Glucosidases