Lysosomal storage diseases (LSDs) cause a toxic buildup that damages your body’s cells and organs. Researchers have found more than 70 types of LSDs. Providers usually diagnose LSDs during pregnancy or infancy. Diagnosis includes blood and urine tests. Treatments include enzyme replacement therapy, stem cell transplants and medications.
Lysosomal storage diseases are inherited metabolic disorders. Most LSDs are autosomal recessive disorders. You must inherit a changed (mutated) gene from each parent for you to develop an LSD. Your parents carry these gene mutations, but they don’t have a lysosomal storage disease.
When both of your parents have a mutated gene, you have a:
In some conditions, only one parent may carry this gene mutation (X-linked inheritance). Three LSDs have X-linked inheritance:
Lysosomal storage diseases may also get triggered by:
Symptoms of lysosomal storage disease vary based on the:
Symptoms commonly found in many types of lysosomal storage disorders include:
Homoeopathy today is a rapidly growing system and is being practiced all over the world. It strength lies in its evident effectiveness as it takes a holistic approach towards the sick individual through promotion of inner balance at mental, emotional, spiritual and physical levels. When is concerned there are many effective medicines available in Homoeopathy , but the selection depends upon the individuality of the patient , considering mental and physical symptoms
Few homoeopathic medicine can be thought of in the treatment of Lysosomal storage diseases are:
ceonathus, cardus mar., chelidonium, lycopodium, nux vom., etc.