Alport Syndrome Market

Alport Syndrome Market Research Report 2032

DelveInsight's "Alport Syndrome Market Insights, Epidemiology and Market Forecast 2032" report delivers an in-depth understanding of the Alport Syndrome, historical and forecasted epidemiology as well as the Alport Syndrome market trends in the United States, EU5 (Germany, Spain, Italy, France, and United Kingdom) and Japan.

Some of the facts of the Alport Syndrome Market report:

· Alport syndrome occurs in approximately 1 in 50,000 newborns.

· Alport syndrome is estimated to account for 3% of children with chronic kidney disease and 0.2% of adults with end-stage renal disease in the United States.

· Alport Syndrome is estimated to affect approximately 1 in 5,000-10,000 people in the general population in the United States.

Key benefits of the Alport Syndrome Market Report

· Alport Syndrome market report covers a descriptive overview and comprehensive insight of the Alport Syndrome epidemiology and Alport Syndrome market in the 7 MM (the United States, EU5 (Germany, Spain, France, Italy, UK) & Japan.)

· Alport Syndrome market report provides insights on the current and emerging therapies.

· Alport Syndrome market report provides a global historical and forecasted market covering drug outreach in 7 MM.

· Alport Syndrome market report offers an edge that will help in developing business strategies by understanding trends shaping and driving the Alport Syndrome market.

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"According to DelveInsight, Alport syndrome primarily affects men."

Alport Syndrome (also referred to as hereditary nephritis) is an inherited progressive form of glomerular disease that is often associated with sensorineural hearing loss and ocular abnormalities. Patients with Alport Syndrome will experience progressive loss of kidney function. Almost all patients experience blood in their urine (hematuria) as well as proteinuria at symptom onset. The kidneys lose function as this condition progresses, resulting in kidney failure. There are three genetic Sub-divisions. X-linked Alport Syndrome (XLAS) is the most common; in these families affected males typically have more severe disease than affected females.

In autosomal recessive Alport Syndrome (ARAS) the severity of disease in affected males and females is similar. There is also an autosomal dominant form (ADAS) that affects males and females with equal severity. Alport Syndrome is caused by mutations in specific genes.

People with Alport Syndrome frequently develop sensor neural hearing loss, which is caused by abnormalities of the inner ear, during late childhood or early adolescence. Affected individuals may also have misshapen lenses in the eyes (anterior lenticonus) and abnormal coloration of the light- sensitive tissue at the back of the eye (retina). These eye abnormalities seldom lead to vision loss.

"According to DelveInsight, Significant hearing loss, eye abnormalities, and progressive kidney disease are more common in males with Alport Syndrome than in affected females. "

The launch of the emerging therapies is expected to significantly impact Alport Syndrome treatment scenario in the upcoming years:-

Alport Syndrome Drugs covered

· RG 012

· SAR339375

· Bardoxolone Methyl

· Atrasentan

· And many others

Alport Syndrome Companies are:

· Regulus Therapeutics

· Sanofi Genzyme

· Reata Pharmaceuticals

· Novartis

· Chinook Therapeutics

· And many others

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