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Waiting Time - 22-25 Working Days

(Earlier appointment depends on the availability of slots) Consultation will be given through audio call.

Ayurvedic Treatment of Fabry Disease

Fabry Disease Treatment in Medical Astrology

Fabry disease, also known as Anderson-Fabry disease, is a rare genetic disorder that affects multiple organs, including the kidneys, heart, and skin. It falls under the category of lysosomal storage diseases. Ayurvedic treatment of Fabry disease involves the use of specific herbs and natural remedies to help manage the condition.This disease results from a genetic mutation that interferes with the function of an enzyme, leading to the accumulation of biomolecules called sphingolipids. These substances build up in the walls of blood vessels and other organs, causing significant health complications. Fabry disease is inherited in an X-linked manner.

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Fabry disease can be diagnosed using a blood test that measures the activity of the affected enzyme called alpha-galactosidase. However, in females, genetic testing is also recommended.

Treatment Approaches:

  • The treatment varies depending on the affected organs.
  • The underlying cause can be addressed by replacing the missing enzyme.

What is the Underlying Principle of Fabry Disease?

Fabry disease is an X-linked lysosome disorder that leads to excessive deposition of neutral glycosphingolipids in various organs, including the vascular endothelium, epithelial cells, and smooth muscle cells. It is a rare and inherited disease that can have life-threatening consequences.

Organs Affected:

  • Heart
  • Lungs
  • Kidneys
  • Skin
  • Stomach
  • Brain

Who is Affected by Fabry Disease?

Fabry disease affects both males and females across all ethnic groups. However, men are usually more severely affected than women.

Types of Fabry Disease

  1. Type 1 Fabry Disease (Classic FD) – Begins in childhood and is less common.
  2. Type 2 Fabry Disease – Develops later in life and is more common.

Other Names for Fabry Disease:

  • Galactosidase Alpha Gene Deficiency
  • Enzyme Alpha-Galactosidase A Deficiency
  • Angiokeratoma Corporis Diffusum
  • Ceramide Trihexosidase Deficiency

Symptoms of Fabry Disease

Common Symptoms:

  • Burning sensation in hands and feet
  • Tingling pain in limbs
  • Skin rash
  • Dizziness and general fatigue
  • Damage to blood vessels in the eyes
  • Reduced sweat production
  • Intense body pain
  • Cramps, gas, and diarrhea
  • Stomach problems
  • Heart enlargement and irregular heartbeat
  • Thickening of heart muscle and heart failure

Other Symptoms:

  • Fever
  • Hearing loss
  • Lung disease
  • Ringing in the ears (tinnitus)
  • Inability to perform strenuous exercise

What Population is Affected by Fabry Disease?

Fabry disease is relatively rare, but its prevalence has been studied:
  • The U.S. population in 2016 was estimated to be 323 million.
  • Type 1 Fabry Disease affects approximately 1 in 40,000 males.
  • Type 2 Fabry Disease occurs in 1 out of 1,500 to 4,000 males.

Ayurvedic Treatment of Fabry Disease

Fabry disease is a genetic disorder, but it can be managed through Ayurveda. Ayurveda, an ancient healing system, focuses on treating diseases using herbal remedies derived from nature.

Ayurvedic Approach:

  • Uses herbs, tree bark, and roots for treatment.
  • Ayurveda identifies RASAYAN in the human body, similar to Ayurvedic herbs.
  • Ayurvedic herbs have the potential to heal defective genes, reducing the intensity of the disease.

Medical Astrology Consultation

If you are struggling with Fabry disease or any other difficult-to-treat disorder, you can consult our Medical Astrologer - Prashant Kapoor for guidance.
Book your consultation today!Waiting time: 22-25 working days (Earlier appointments depend on slot availability).Consultation will be provided through audio call.
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