Fabry disease, also known as Anderson-Fabry disease, is a rare, inherited condition. The disease affects the body's ability to produce enough of an enzyme called alpha-galactosidase A (alpha-GAL A). It is classified as a lysosomal storage disorder, which can cause damage to the body's organs and cells.
Although it affects 1 in 40,000 to 1 in 117,000 live births in India, knowledge and awareness about the condition are crucial. Fortunately, the top hospitals in Noida have treatment facilities available for rare conditions like Fabry disease.
However, the type of treatment depends on the severity of the disease. Keep reading to explore the treatment options for Fabry disease in Noida.
There is no known cure for the Anderson-Fabry disease. The disease has a lot of complications, which require medical attention from time to time. Treatments for Fabry disease in Noida are:
However, this treatment can be expensive; for example, a single 3.5 mg vial may cost approximately ₹1,80,000 to ₹2,00,000, depending on procurement source.
In addition to the treatments, doctors may suggest further measures to manage the various symptoms associated with Fabry disease. These include:
Fabry disease can affect various parts of the body. Thus, regular monitoring becomes crucial, which generally involves:
Any reputed hospital or diagnostic centre in Noida provides these services. Noida has world-class super-speciality hospitals, offering access to doctors from various departments. The basic fees of the doctors can range from ₹600 to ₹2000.
Fabry disease is a rare and complex disease. Understanding more about it and its treatments helps with early detection. Therefore, quality of life can significantly improve through regular medical management and enzyme replacement.