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Providers may evaluate markers such as P1NP (procollagen type I N-terminal propeptide) to guide initial titration
Such as thymosin beta-4 derivatives, Cerebrolysin, or Dihexa
These additional causes include sporadic genetic disorders, such as spinocerebellar atrophy type 27B, caused by GAA expansion in the FGF14 gene, and cerebellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS), caused by biallelic expansions in the RFC1 gene
Many other factors could explain the results
Transparency is also important
doi:10.1016/j.jgr.2020.11.002 Irfan M, Jeong D, Saba E, et al
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