Larsons' Homeo - Familial Lipoprotein Lipase Deficiency


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Familial Lipoprotein Lipase Deficiency

Treatment No. :	RD0209
Dosage & Instructions:	15 drops in 15 ml of plain water twice a day, mornings and evenings.
Composition:	Atropine sulph D200+200C Belladonna D200+200C Dioscorea D200+200C Fel tauri D30+100C Iris versicolor D200+200C Merc sol D200+200C Pancreatinum D200+200C
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:

Familial lipoprotein lipase deficiency is a rare hereditary enzyme deficiency that results in abnormal breakdown of fats in the body. It is characterized by a massive accumulation of fatty droplets (chylomicrons) in blood plasma and a corresponding increase of the blood plasma concentration of fatty substances called triglycerides. The disorder is caused by a mutation in the LPL gene leading to very low or absent activity of the lipoprotein lipase enzyme.

Symptoms of familial LPL deficiency usually begin in childhood and include abdominal pain, acute and recurrent inflammation of the pancreas (pancreatitis), skin lesions called eruptive cutaneous xanthoma and an enlargement of the liver and spleen (hepatosplenomegaly).

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Larsons Homeo
Suite 3587
SE-111 74 Stockholm
Sweden