Larsons' Homeo - Pompe Disease


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Pompe Disease

Treatment No. :	RD0691
Dosage & Instructions:	15 drops in 15 ml of plain water twice a day, mornings and evenings before meal.
Composition:	Basilicum D2 Vinca minor D3 Asa foetida D3 Podophyllinum D4 China D3 Chamomilla D3 Sulfur D4 Lycopodium D4 Colchicum D4 Belladonna D3
Treatment Type:	This remedy is a symptomatic treatment. A symptomatic treatment cannot eliminate the disease from its root but is able to considerably improve the patient's condition by easing his or her symptoms.
Contra-indications:	None established
Special Instructions:	Whereas this remedy can be safely used by teenagers, its use has not been evaluated in children under 12 years of age. Please do not administer to children under this age.
Storage:	Store in a cool and dry place
Precautions:	Keep away from the reach of children
Standard Packaging :	30 ml Drops
Order Online:	One 30 ml bottle for $79.99 Two 30 ml bottles for $129.99

Condition Overview:

Pompe disease is a hereditary metabolic disorder caused by the complete or partial deficiency of the enzyme acid alpha-glucosidase (also known as lysosomal alpha-glucosidase or acid maltase). This enzyme deficiency causes excess amounts of glycogen to accumulate in the lysosomes of many cell types but predominantly in muscle cells. The resulting cellular damage manifests as muscle weakness and/or respiratory difficulty.

There are 49 rare genetic disorders known as lysosomal storage diseases, and Pompe disease is one of them. It is also classified as glycogen storage disease type II (GSD II).
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Larsons Homeo
Suite 3587
SE-111 74 Stockholm
Sweden