Larsons' Homeo - Carnitine Palmitoyltransferase Deficiency


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Carnitine Palmitoyltransferase Deficiency

Treatment No. :	RD0137
Dosage & Instructions:	15 drops in 15 ml of plain water twice a day, mornings and evenings.
Composition:	Dysentery co. D200+200C Cortisone D200+200C Mucor Mucedo D200+200C Cals phos D200+200C Crocus sat D200+200C Cup met D200+200C Zinc met 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:

Carnitine Palmitoyltransferase (CPT) Deficiency is a very rare metabolic disorder that affects the skeletal muscles and their ability to function properly. CPT Deficiency belongs to a group of diseases that involve the defective breakdown (metabolism) of muscle fats (lipids). Prolonged periods of strenuous exercise can trigger an episode of symptoms. These may include muscle aches, stiffness, and weakness. Muscle tissue may break down (rhabdomylosis) and abnormal levels of myoglobulin may be present in the urine (myoglobinuria). The urine may appear dark reddish-brown after prolonged periods of exercise.

Carnitine Palmitoyltransferase (CPT) Deficiency Type 1 typically affects adults and adolescents. Carnitine Palmitoyltransferase (CPT) Deficiency Type 2 may also affect adults; however, a serious form of this type of the disease affects infants.
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Larsons Homeo
Suite 3587
SE-111 74 Stockholm
Sweden