Allopathic Medications for Genes Cure
Allopathic medications play a vital role in managing genetic disorders by targeting symptoms and improving patient quality of life. At Genes Cure, we provide comprehensive information on effective medications that align with the latest medical advancements, helping patients and healthcare providers make informed decisions for optimal genetic health outcomes.
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Cystic fibrosis
Brief information about it: Cystic fibrosis (CF) is a genetic disorder that affects the lungs and other organs. It is…
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Hemophilia B
Brief information about it: Hemophilia B is a rare genetic disorder that causes a deficiency in clotting factor IX, a…
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Leber congenital amaurosis (LCA) type 2
Brief information about it: Leber congenital amaurosis (LCA) type 2 is a rare genetic disorder that causes vision loss from…
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Spinal muscular atrophy (SMA)
Brief information about it: Spinal muscular atrophy (SMA) is a genetic disorder that affects the motor neurons, which are nerve…
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Lipoprotein lipase deficiency (LPLD)
Brief information about it: Lipoprotein lipase deficiency (LPLD) is a rare genetic disorder that affects the metabolism of fats. People…
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Sanfilippo syndrome type A
Brief information about it: Sanfilippo syndrome type A is a rare genetic disorder caused by a deficiency of the enzyme…
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Hunter syndrome
Brief information about it: Hunter syndrome is a rare genetic disorder caused by a deficiency of the enzyme iduronate-2-sulfatase (IDS).…
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Fabry disease
Brief information about it: Fabry disease is a rare genetic disorder caused by a deficiency of the enzyme alpha-galactosidase A…
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Pompe disease
Brief information about it: Pompe disease is a rare genetic disorder caused by a deficiency of the enzyme acid alpha-glucosidase…
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Enzyme Replacement Therapy (ERT)
Gaucher disease Brief information about it: Ceredase is an enzyme replacement therapy (ERT) used to treat Gaucher disease, a rare…
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