Gaucher disease is a lysosomal storage disorder that is autosomal recessive and is characterised by a deficiency in the lysosomal enzyme glucocerebrosidase that is required in the breakdown of the glycolipid glucocerebroside (glucosylceramide).
More information on Gaucher disease.
All content and media on the HealthEngine Blog is created and published online for informational purposes only. It is not intended to be a substitute for professional medical advice and should not be relied on as health or personal advice. Always seek the guidance of your doctor or other qualified health professional with any questions you may have regarding your health or a medical condition. Never disregard the advice of a medical professional, or delay in seeking it because of something you have read on this Website. If you think you may have a medical emergency, call your doctor, go to the nearest hospital emergency department, or call the emergency services immediately.
