DelveInsight’s “Phenylketonuria (PKU) Market Insights Report” offers a detailed analysis of the disease, its causes, symptoms, diagnostics, modalities, and treatment options.
The Phenylketonuria market report also covers Phenylketonuria market size, epidemiology, developing medicines, market drivers, market hurdles, ongoing clinical studies, significant partnerships in the sector, and key pharmaceutical companies actively driving the Phenylketonuria market size forward.
Some of the key highlights from the Phenylketonuria Market Insights:
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Phenylketonuria is a metabolic disorder that can be detected during the first few days of life through regular newborn screening. The enzyme phenylalanine hydroxylase (PAH), which is responsible for digesting the amino acid phenylalanine, is absent or deficient in Phenylketonuria.
Proteins’ chemical building blocks, amino acids, are required for normal growth and development. Phenylalanine is metabolized to tyrosine in the presence of normal PAH activity. When PAH is missing or insufficient, phenylalanine builds up and becomes toxic to the brain.
Most patients with Phenylketonuria would have a serious intellectual handicap if they were not treated. Treatment begins during the early days or weeks of infancy with a carefully managed, phenylalanine-restricted diet to prevent intellectual impairment.
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Phenylketonuria Epidemiology Segmentation
The Phenylketonuria Market report proffers epidemiological analysis for the study period 2017-30 in the 7MM segmented into:
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There is currently no cure for phenylketonuria, however, the most common treatment is a dietary restriction of phenylalanine to the bare minimum required for proper growth, supplemented with specially tailored medical meals.
For many years, the only treatment for Phenylketonuria was to follow a strict low-phenylalanine diet for the rest of one’s life. As a result, the primary line of treatment for Phenylketonuria is dietary therapy, which begins soon after diagnosis and consists of a low Phe diet supplemented with amino acid formulations.
The goal of Phenylketonuria treatment is to keep plasma phenylalanine levels between 120 and 360 mol/L (2–6 mg/dL), which can be accomplished with a properly designed and supervised diet. Because phenylalanine is an important amino acid, it should be limited in the child’s diet. A well-balanced diet can help people avoid intellectual handicaps, as well as neurological, behavioral, and dermatological issues.
Pharmaceutical companies’ extensive research and development activities, already approved therapies, and expanding prevalence will all contribute to the growth of the Phenylketonuria market.
Phenylketonuria Pipeline Therapies and Key Companies
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Phenylketonuria Market Drivers
Scope of the Report
Key Questions Answered in the Report
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Table of Contents
|3.||Phenylketonuria Competitive Intelligence Analysis|
|4.||Phenylketonuria Market Overview at a Glance|
|5.||Phenylketonuria Executive Summary|
|6.||Phenylketonuria Epidemiology and Market Methodology|
|7.||Phenylketonuria Epidemiology and Patient Population|
|8.||Phenylketonuria Patient Journey|
|9.||Treatment Algorithm, Current Treatment, and Medical Practices|
|10.||Key Endpoints in Phenylketonuria Clinical Trials|
|11.||Phenylketonuria Marketed Therapies|
|12.||Phenylketonuria Emerging Therapies|
|13.||Phenylketonuria: 7 Major Market Analysis|
|15.||Phenylketonuria Access and Reimbursement Overview|
|18.||Phenylketonuria Market Drivers|
|19.||Phenylketonuria Market Barriers|
Learn more about the report offerings @ Phenylketonuria Market Outlook
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