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tested remedies | Most affordable prices
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Moyamoya Syndrome
| Treatment No. : |
RD0487 |
| Dosage & Instructions: |
15 drops in 15 ml of plain water twice a day,
mornings and evenings.
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| Composition: |
Viscum alb D1+10C
Crataegus oxy D1+10C
Baryta carb D6+60C
Aurum mur D6+60C
Ars alb D6+60C
Aurum lod D6+60C
Baryta lodata D6+60C |
| 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.
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| 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.
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| Storage: |
Store in a cool and dry place |
| Precautions: |
Keep away from the reach of children |
| Standard Packaging : |
30 ml Drops |
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Order Online:
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One 30 ml bottle for $79.99
Two 30 ml bottles for $129.99
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Condition Overview: Moyamoya syndrome is a progressive disorder that affects the blood vessels in the brain (cerebrovascular). It is characterized by the narrowing (stenosis) and/or closing (occlusion) of the carotid artery, the major artery that delivers blood to the brain. Inadequate blood supply leads to reduced oxygen to the brain, and it is this oxygen deprivation that causes the signs of Moyamoya. Those signs most typically include paralysis of the feet, legs or the upper extremities. Headaches, various vision problems, mental retardation, and psychiatric problems may also occur.
Approximately 10% of cases of Moyamoya syndrome are due to a genetic cause and are termed primary Moyamoya syndrome. Secondary Moyamoya syndrome refers to cases in which the syndrome is a consequence or result of another underlying disorder. In secondary Moyamoya syndrome, when it is not a result of a genetic cause, it is important for the physician to determine the root underlying cause. .
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