Gaucher Disease (GD) - Market Insights, Epidemiology and Market Forecasts, 2024

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Gaucher Disease (GD) - Market Insights,
Epidemiology and Market Forecasts, 2024
The Report,” Gaucher Disease - Epidemiology Forecast to 2024" market research providing an overview
of the risk factors and global trends of GD in the 7MM US, France, Germany, Italy, Spain, UK, and Israel.
It includes a 10-year epidemiology forecast for the total prevalent cases of Type 1, 2, and 3 GD,
segmented by age and sex in these markets. GD epidemiology report is written and developed by
Masters- and PhD-level epidemiologists. The EpiCast Report is in-depth, high quality, transparent and
market-driven, providing expert analysis of disease trends in the 7MM.
The Report on Gaucher Disease is in-depth, high quality, transparent and market-driven, providing expert
analysis of disease trends in the 7MM.
Browse detailed TOC, Tables, figures, Charts and Companies mentioned in Gaucher Disease –
Epidemiology Forecast Report at- http://www.marketreportsworld.com/epicast-report-gaucher-diseaseepidemiology-forecast-to-2024-10077055
Epidemiologists forecast that the total prevalent cases of Type 1 GD in the 7MM will increase from 12,036
cases in 2014 to 13,006 cases in 2024, with the majority of cases occurring in the US and Israel. Types 2
and 3 GD are even more rare than Type 1, with only 121 cases of Type 2 and 613 cases of Type 3
across the 7MM in 2014. Epidemiologists predict that the total prevalent cases of Type 2 GD in the 7MM
will increase from 121 cases in 2014 to 125 cases in 2024, and that the total prevalent cases of Type 3
GD in the 7MM will increase from 613 cases in 2014 to 640 cases in 2024. The disease affects men and
women in equal numbers across the 7MM.
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Gaucher Disease (GD) is a rare, inherited lysosomal storage disorder (LSD) that is classified into three
forms - Types 1, 2, and 3 - which are distinguished by their symptoms, severity, and neurological
involvement. GD affects the ability of cells to break down a specific type of fat, glucocerebroside (GC), as
a result of the deficiency or limited activity of the enzyme glucocerebrosidase (GCase). This leads to the
harmful accumulation of GC, which is also known as glucosylceramide, in the lysosomes, most commonly
in the macrophages and monocytes, throughout the body. The most significant difference between the
three types of GD is whether or not there is neurological involvement.
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