Larsons' Homeo - Cystinuria


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Cystinuria

Treatment No. :	RD0169
Dosage & Instructions:	15 drops in 15 ml of plain water twice a day, mornings and evenings.
Composition:	Ber vulg 0+10C Nat oxalaceti D100+100C Solidago vir 0+10C Stigmata maydis 0+10C Thlaspi.B.P 0+10C Calcarea renalis D100+100C Parathormone D30+30C
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:

Cystinuria is an inherited metabolic disorder characterized by the abnormal movement (transport) in the intestines and kidneys, of certain organic chemical compounds (amino acids). These include cystine, lysine, arginine, and ornithine. Excessive amounts of undissolved cystine in the urine (cystinuria) cause the formation of stones (calculi) in the kidney, bladder, and/or ureter.

Four subtypes of Cystinuria are recognized. In Type I Cystinuria, there is a defect in the active transport of cystine and the amino acids (dibasic) lysine, arginine, and ornithine in the kidneys and small intestine. People who are carriers of the gene for this type of the disorder generally have no symptoms. In Type II Cystinuria, cystine and lysine transport is severely impaired in the kidneys and only somewhat impaired in the intestines. In Type III Cystinuria, kidney transport of cystine and lysine is defective; intestinal transport is normal. People who are carriers of the gene for this variety of the disease typically have slightly elevated levels of cystine and lysine in the urine. In Hypercystinuria, there is generally a moderate elevation of cystine in the urine; intestinal absorption of cystine and the dibasic amino acids is normal.

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Larsons Homeo
Suite 3587
SE-111 74 Stockholm
Sweden