Sep 30, 2026 · 20 min · 8 segments
Welcome to the *NeurologyLive*® Mind Moments® podcast. Tune in to hear leaders in neurology sound off on topics that impact your clinical practice. In this special episode of *Mind Moments*, released…
Katherine MathewsGuest
Marco MeglioHost
This drug is being developed for treating one specific type of limb girdle muscular dystrophy called LGMDR9.

This is a recessive form of muscular dystrophy that is caused by mutations in the gene FKRP or Fucatin-related protein.

So what FKR, so LGMDR9 is one of a group of disorders called the distroglycanopathies that share a common pathological mechanism that is a hypoglycosylation of alpha-distroglycan.

So alpha-distroglycan is part of the dystrophin glycoprotein complex that connects the inside the cell to the extracellular matrix and provides stability for the muscle cell membrane.

That complex requires extensive glycosylation of alpha-dystroglycan in order to connect to the extracellular matrix.

So if it is dysfunctional, that glute chain is truncated and dysfunctional and doesn't work as well.

The concept here is that if you can add the precursor sugar an excess of the precursor form of ribitol that FKRP works on, that you can make the residual FKRP activity work harder and thus get more extension of the glucose chains on alpha-dystroglycan.

and why it's really, this is not going to be a general therapy for limb girdle muscular dystrophies.

This drug is being developed for treating one specific type of limb girdle muscular dystrophy called LGMDR9.

This is a recessive form of muscular dystrophy that is caused by mutations in the gene FKRP or Fucatin-related protein.

So what FKR, so LGMDR9 is one of a group of disorders called the distroglycanopathies that share a common pathological mechanism that is a hypoglycosylation of alpha-distroglycan.

So alpha-distroglycan is part of the dystrophin glycoprotein complex that connects the inside the cell to the extracellular matrix and provides stability for the muscle cell membrane.

That complex requires extensive glycosylation of alpha-dystroglycan in order to connect to the extracellular matrix.

So if it is dysfunctional, that glute chain is truncated and dysfunctional and doesn't work as well.

The concept here is that if you can add the precursor sugar an excess of the precursor form of ribitol that FKRP works on, that you can make the residual FKRP activity work harder and thus get more extension of the glucose chains on alpha-dystroglycan.

and why it's really, this is not going to be a general therapy for limb girdle muscular dystrophies.
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