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After that, most patients pay approximately $140-$165 per month total (membership + medication at cost) for the first 3 months

Mutations in the ABHD5 gene result in the lipid storage myopathy (LSM) identified as neutral lipid storage disease with ichthyosis, NLSDI, also known as Chanarin-Dorfman syndrome

The lack of FDA approval for human use and the need for higher doses in some experimental settings underscore the importance of evaluating safety and efficacy under strict medical supervision