Genetics and its impact on medicine

by Alleviare Life Sciences Private Limited Way Towards New Life

What is Genetics?

A disorder caused by anomalies in the individual genome. Examples include cystic fibrosis Falcille anemia Marfan syndrome Huntington as well as Hemochromatosis. Genetically unique disorders are identified in well-known models: Autosomal dominance, automatic diving, and linked.

There are three kinds in genetic diseases:

* Disruptions that are distributed, in which mutations alter genes. A good example is sickle cell disease.

* Chromosomal diseases, that are when the chromosomes (or components of the chromosomes) are absent or altered. ...

* Complex disorders, in which the mutations are in more than one gene.

Genetic Drugs

Cystagon (Cysteamine Bitartrate)

Cysteamine is a catalyst for breaking down cystine within the body. The medicine is prescribed to help treat cysts in the kidneys both in both adults and children. The medicine helps maintain kidney function and to control kidney damage as well as other conditions in those with an inheritable condition which causes a naturally occurring compound (cystine) to accumulate within our bodies (cystine) kidney cyst).

(Form & Strength): 50mg, 150mg

Cerdelga (Eliglustat)

Cerdelga is a prescribed drug that is used to treat the long-term effects of adult Gaucher's Disease type 1 (GD1). The metabolites that are ultra-fast of CYP2D6 are not capable of achieving sufficient levels of Serderga to create the therapeutic effects. It is not recommended to take a specific dose for the undetermined CYP2D6 metabolisms.

(Form and Strength) : 84 mg, orally, once a day.

Zavesca

Zavesca is used for treating mild to moderate Gaucher's disease in patients that are not receiving treatment with enzyme replacement therapy. Zavesca is recommended to treat adults with oral medication patients with moderate to mild Gaucher's disease of type 1.

Zavesca should be used only to treat patients not suitable for replacement enzyme therapy.

(Form and Strength): Capsule 100mg

Elaprase (Idursulfase)

Elaprase is a prescribed drug for people suffering from Hunter's Syndrome. It has been demonstrated that Elaprase can enhance walking abilities in patients who are older than five years. Idursulfase is a natural enzyme which are insufficient due to hereditary issues. Eraplase is a replacement for this enzyme that is deficient. (Form and strength) Inject 6 mg/3 milliliters (2 mg/ml) into an empty vial.

Carbaglu

Carbaglu is a medication that contains Carglumic Acid, the main ingredient. It is dispersible tablets. "Dispersity" means that tablets are able to become dispersed (mixed) within water.

Carbaglu is a treatment for excessive ammonemia (high concentrations of ammonia present in blood) in patients suffering from the following metabolic conditions: N-acetylglutamate synthase (NAGS) insufficient. Patients suffering from this chronic condition generally have a liver enzyme that is called NAGS, which helps in breaking down ammonia.

In the event that the enzyme is insufficient ammonia can't be broken down and builds up in blood. There are some organic acidemias (isovaleric acidemia as well as methylmalonic acidemia and propionic acidemia) where the patient does not have specific enzymes that are that play a role in metabolism of protein.

(Form as well as strength) (Form and strength): 200 mg tablet

Normosang (Human-Hemin)

Normosang is a treatment for acute attacks that happen in patients who suffer with acute porphyria of the liver. The condition is defined by the accumulation of toxins in the liver (including porphyrin as well as the toxic components).

There are three kinds of liver porphila.

Acute intermittent porphyria

* Porphyria variegata,

* Hereditary Coropropolia.

This can cause symptoms of the disease which include discomfort (mainly stomach, backrest thighs) nausea, vomiting, and constipation.

(Form and Strength): Normosang Injection 250MG

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