Pompe disease (GSD type II): other management
Evidence-based neurology checklist on pompe disease (gsd type ii): other management: General Provide patient information Early treatment of infections Treat co-morbidities Enzyme replacement therapy Physical Systemic Nutritional Immunizations Anaesthesia management Genetic counselling: issues
General
- Provide patient information
- Early treatment of infections
- Treat co-morbidities
- Enzyme replacement therapy
Physical
Systemic
Nutritional
Immunizations
Anaesthesia management
Genetic counselling: issues
References
- Bembi B, Cerini E, Danesino C, et al. Diagnosis of glycogenosis type II. Neurology 2008; 71(Suppl 2):S4-S11.
- Kishani PS, Steiner RD, Bali D, et al. Pompe disease diagnosis and management guideline. ACGM Practice guideline 2006; 8:5.
- Llerena JC Jr, Horovitz DM, Marie SK, et al. The Brazilian consensus on the management of Pompe disease. J Pediatr 2009; 155(4 Suppl):S47-S56.
- Taglia A, Picillo E, D'Ambrosio P, Cecio MR, Viggiano E, Politano L. Genetic counseling in Pompe disease. Acta Myol 2011; 30:179-181.
- Stevens D, Milani-Nejad S, Mozaffar T. Pompe disease: a clinical, diagnostic, and therapeutic overview. Curr Treat Options Neurol 2022; 24:573-588.
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