Latin America Fabry Disease Treatment Market Expected to Reach USD 164.68 Million by 2034 with 6.6% CAGR
- prajwal79
- Oct 17
- 3 min read
Market Overview
Global Latin America Fabry Disease Treatment Market size and share is currently valued at USD 81.36 million in 2024 and is anticipated to generate an estimated revenue of USD 164.68 million by 2034, according to the latest study by Polaris Market Research. Besides, the report notes that the market exhibits a robust 6.6% Compound Annual Growth Rate (CAGR) over the forecasted timeframe, 2025 - 2034
The Latin America Fabry disease treatment market is witnessing growth due to increasing awareness of rare genetic disorders, advances in therapeutic options, and improved healthcare infrastructure in the region. Fabry disease is a rare, inherited lysosomal storage disorder caused by a deficiency of the enzyme alpha-galactosidase A, leading to the accumulation of harmful substances in the body. The market includes enzyme replacement therapies (ERT), chaperone therapies, gene therapies, and supportive treatments aimed at managing symptoms and slowing disease progression. Rising diagnosis rates and growing access to specialized treatments are driving market expansion.
𝐄𝐱𝐩𝐥𝐨𝐫𝐞 𝐓𝐡𝐞 𝐂𝐨𝐦𝐩𝐥𝐞𝐭𝐞 𝐂𝐨𝐦𝐩𝐫𝐞𝐡𝐞𝐧𝐬𝐢𝐯𝐞 𝐑𝐞𝐩𝐨𝐫𝐭 𝐇𝐞𝐫𝐞: https://www.polarismarketresearch.com/industry-analysis/latin-america-fabry-disease-treatment-market
Growth Drivers
Several factors are fueling growth in the Fabry disease treatment market. Increasing awareness of rare genetic disorders and early diagnosis through genetic testing and newborn screening programs drive demand for targeted therapies. Advancements in enzyme replacement therapies and emerging gene therapies offer improved efficacy and better patient outcomes. Government initiatives, health insurance coverage, and reimbursement programs in countries like Brazil, Mexico, and Argentina support adoption of high-cost therapies. Additionally, growing patient advocacy, specialized treatment centers, and increasing clinical research activities enhance access to treatment and market growth.
Market Challenges and Opportunities
Challenges in the Latin America Fabry disease treatment market include high treatment costs, limited access to specialized therapies, and scarcity of healthcare professionals trained in rare diseases. Low disease awareness in rural areas and delayed diagnosis may also affect market growth. However, these challenges create opportunities for innovative, cost-effective therapies, telemedicine consultations, and educational programs for healthcare providers and patients. Emerging opportunities also exist in expanding access to gene therapies, orphan drugs, and public-private partnerships to improve treatment availability across the region.
𝐌𝐚𝐣𝐨𝐫 𝐊𝐞𝐲 𝐂𝐨𝐦𝐩𝐚𝐧𝐢𝐞𝐬:
Chiesi Farmaceutici S.p.A.
JCR Pharmaceuticals Co., Ltd.
Protalix BioTherapeutics Inc.
Sanofi
Takeda Pharmaceutical
Amicus Therapeutics, Inc.
Idorsia Pharmaceuticals Ltd.
Idorsia Pharmaceuticals Ltd.
ISU ABXIS Co., Ltd.
Sangamo Therapeutics, Inc.
Market Segmentation
The Latin America Fabry disease treatment market can be segmented by therapy type, application, and end-user. Therapy types include enzyme replacement therapy (ERT), chaperone therapy, gene therapy, and supportive care treatments. Applications focus on managing renal, cardiac, neurological, and gastrointestinal symptoms associated with Fabry disease. End-users include hospitals, specialty clinics, diagnostic centers, and homecare providers. Enzyme replacement therapy dominates due to its established efficacy, while gene therapy is emerging as a next-generation treatment with potential long-term benefits. Hospitals and specialty clinics remain the primary end-users for diagnosis, treatment, and monitoring of patients.
Regional Analysis
Brazil leads the Fabry disease treatment market in Latin America due to advanced healthcare infrastructure, government initiatives, and growing adoption of specialized therapies. Mexico follows, with increasing awareness programs, access to rare disease centers, and supportive reimbursement schemes. Argentina is gradually adopting Fabry disease therapies through hospital networks and private clinics. Other countries in the region are emerging markets, supported by regional awareness campaigns, clinical research programs, and expanding access to rare disease treatments.
Summary of PR
The Latin America Fabry disease treatment market is expanding due to increasing disease awareness, advances in therapies, and improved healthcare access. Challenges such as high treatment costs, limited specialist availability, and delayed diagnosis are fostering innovation in cost-effective therapies, telemedicine support, and patient education initiatives. Segmentation includes therapy type, application, and end-users, reflecting adoption across enzyme replacement therapy, chaperone therapy, gene therapy, hospitals, specialty clinics, and diagnostic centers. Brazil and Mexico lead adoption, while other countries in Latin America offer growth potential. Continued clinical research, healthcare investments, and patient advocacy are expected to sustain market growth across the region.
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