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Sanfilippo syndrome refers to a group of inherited lysosomal storage disorders that primarily affect a child's central nervous system, including the brain and spinal cord. It is rare, affecting an estimated 1 in every 50,000 to 250,000 people. Type A is the most common subtype worldwide, while type D is the least common.
Base Year
Historical Period
Forecast Period

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Expert Market Research's “Sanfilippo Syndrome Epidemiology Forecast Report 2026-2035” offers comprehensive information on the prevalence and demographics of Sanfilippo syndrome. It projects the future incidence and prevalence rates of Sanfilippo syndrome across various populations. The study covers age and type as major determinants of the Sanfilippo syndrome-affected population. The report highlights patterns in the prevalence of Sanfilippo syndrome over time and projects future trends based on multiple variables.
The report provides a comprehensive overview of the disease, as well as historical and projected data on the epidemiology of Sanfilippo syndrome in the 8 major markets.
Regions Covered
Sanfilippo syndrome falls under the category of lysosomal storage diseases, primarily affecting the central nervous system. The disorder is caused by a deficiency in specific enzymes needed to break down complex sugars in the body. This leads to the accumulation of these substances in cells, particularly in the brain. Children with Sanfilippo syndrome experience developmental delays, hyperactivity, loss of speech, and progressive cognitive decline. The condition also shortens life expectancy, with most children living into their teens or early twenties.
Currently, there is no cure for Sanfilippo syndrome. Medications are usually prescribed to manage symptoms such as seizures, hyperactivity, or sleep disturbances. Physical and occupational therapy help improve motor skills, mobility, and overall functioning as the disease progresses. Speech therapy is also recommended to help with communication issues and can assist in maintaining the child’s ability to express themselves. Researchers are exploring enzyme replacement therapy and gene therapy to address the underlying cause of Sanfilippo syndrome.
The Sanfilippo syndrome epidemiology section offers information on the patient pool from history to the present as well as the projected trend for each of the 8 major markets. Expert Market Research provides both current and predicted trends for Sanfilippo syndrome by examining a wide range of studies. Additionally, the report covers the diagnosed patient pool for Sanfilippo syndrome and their trends. The data is broken down into specific categories, such as the total diagnosed cases across different age groups and patient pools.

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The Sanfilippo syndrome epidemiology data and findings for the United States, Germany, Spain, Italy, France, the United Kingdom, Japan, and India are also provided in the epidemiology section.
The epidemiology of Sanfilippo syndrome varies significantly between countries due to differences in healthcare infrastructure, socioeconomic factors, public awareness of the condition, and population genetics. Variations in the prevalence of the syndrome are also influenced by mutations specific to certain populations. In the United States, Sanfilippo syndrome occurs in approximately 1 in 70,000 births.
Country Specific Stats:
|
Country |
Prevalence (Unit) |
|
United States |
1 in 70,000 births |
|
United Kingdom |
XX |
|
Germany |
XX |
|
Italy |
XX |
|
France |
XX |
|
Spain |
XX |
|
Japan |
XX |
|
India |
XX |
*While we strive to always give you current and accurate information, the numbers depicted on the website are indicative and may differ from the actual numbers in the main report. At Expert Market Research, we aim to bring you the latest insights and trends in the market. Using our analyses and forecasts, stakeholders can understand the market dynamics, navigate challenges, and capitalize on opportunities to make data-driven strategic decisions.*
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Report Features |
Details |
|
Base Year |
2025 |
|
Historical Period |
2019-2025 |
|
Forecast Period |
2026-2035 |
|
Geographies Covered |
|
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