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A rare condition with a slight Middle Eastern link – Acid sphingomyelinase deficiency (ASMD) Orphan genetic diseases afflict a minimal number of people. Relatively rare, they still do affect millions of people, collectively contributing to Global disease burden. Studies conducted estimates that there are as many as 7,000 diseases that are designated as rare, and one out of 15 persons worldwide are estimated to be affected by a rare disease constituting 400 million people worldwide. Around 1 in 5,000 to 10,000 people is the current estimated worldwide incidence of NPD A disease. As per DelveInsight’s analytical report titled, “Acid Sphingomyelinase Deficiency (ASMD) – Market Insights, Epidemiology and Market Forecast-2028 – Emerging Markets”, total prevalent population of ASMD in key Emerging Markets range from 8,799 in 2017 to 9500 in 2028 with a CAGR of 0.70%.
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