Hereditary Transthyretin-Mediated (hATTR) Amyloidosis with Polyneuropathy – Market Outlook, Epidemiology, Competitive Landscape, and Market Forecast Report – 2022 To 2032
Hereditary transthyretin-mediated (hATTR) amyloidosis with polyneuropathy, previously known as familial amyloidotic polyneuropathy, is a rare genetic disorder caused by a mutation in the transthyretin (TTR) gene, which results in the production of abnormal TTR proteins that form amyloid fibrils. The disease is characterized by gradual and progressive degeneration of the autonomic and sensory-motor nervous systems and can be fatal. The symptoms of hATTR amyloidosis with polyneuropathy involve damage to the peripheral and autonomic nervous systems. Peripheral neuropathy usually begins with unusual sensations in the lower limbs, such as numbness, tingling, or burning. Autonomic neuropathy occurs when nerves that control vital functions, such as blood pressure, heart rate, sweating, bladder emptying, and digestion, are damaged. The sensory-motor polyneuropathy in hATTR amyloidosis with polyneuropathy progresses through three stages. In the initial stage, patients typically experience mild sensory symptoms in the lower limbs, but their ability to walk unassisted is preserved. In the second stage, patients require assistance for walking due to the progressive weakness of the lower limb muscles. In the final stage, sensory symptoms are severe, and patients experience flaccid paralysis or severe weakness of all limbs, resulting in the need for a wheelchair or bedridden state. The polyneuropathy disability (PND) score is commonly used to stage the degree of sensory-motor impairment in clinical practice. Patients with PND 0 have no impairment, while those with PND I have sensory disturbances but maintain the ability to walk. Patients with PND II have impaired walking ability but can still walk without a cane or crutch. Patients with PND IIIa require a single cane or crutch, PND IIIb requires two canes or crutches, and PND IV is characterized by wheelchair dependence or bedridden.
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The global prevalence of hereditary
transthyretin-mediated amyloid polyneuropathy was estimated at 38,000
individuals.
Thelansis’s “Hereditary
Transthyretin-Mediated (hATTR) Amyloidosis with Polyneuropathy Market Outlook,
Epidemiology, Competitive
Landscape, and Market Forecast Report – 2021 To 2032" covers disease
overview, epidemiology, drug utilization, prescription share analysis,
competitive landscape, clinical practice, regulatory landscape, patient share,
market uptake, market forecast, and key market insights under the potential Hereditary
Transthyretin-Mediated (hATTR) Amyloidosis with Polyneuropathy treatment
modalities options for eight major markets (USA, Germany, France, Italy, Spain,
UK, Japan, and China).
KOLs insights
of Hereditary Transthyretin-Mediated (hATTR) Amyloidosis with Polyneuropathy
across 8 MM market from the centre of Excellence/ Public/ Private hospitals
participated in the study. Insights around current treatment landscape,
epidemiology, clinical characteristics, future treatment paradigm, and Unmet
needs.
Hereditary Transthyretin-Mediated
(hATTR) Amyloidosis with Polyneuropathy Market Forecast Patient
Based Forecast Model (MS. Excel Based Automated Dashboard), which Data Inputs
with sourcing, Market Event, and Product Event, Country specific Forecast
Model, Market uptake and patient share uptake, Attribute Analysis, Analog Analysis,
Disease burden, and pricing scenario, Summary, and Insights.
Thelansis Competitive Intelligence (CI) practice
has been established based on a deep understanding of the pharma/biotech
business environment to provide an optimized support system to all levels of
the decision-making process. It enables business leaders in forward-thinking
and proactive decision-making. Thelansis supports scientific and commercial
teams in seamless CI support by creating an AI/ ML-based technology-driven
platform that manages the data flow from primary and secondary sources.
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