Two decade wait for medicines for rare genetic disorder
A group representing people with a rare genetic disorder say they've been waiting almost two decades for some critical drugs to be funded. Fabry disease is caused by a missing enzyme, and can lead to life threatening complications including organ failure. There is no cure but there are treatments available overseas to slow degeneration from the disease. Deborah Klyer from Fabry New Zealand spoke to Lisa Owen.
Checkpoint · RNZ
March 27, 20267m 4s
Audio is streamed directly from the publisher (flex.acast.com) as published in their RSS feed. Play Podcasts does not host this file. Rights-holders can request removal through the copyright & takedown page.
Show Notes
A group representing people with a rare genetic disorder say they've been waiting almost two decades for some critical drugs to be funded. Fabry disease is caused by a missing enzyme, and can lead to life threatening complications including organ failure. There is no cure but there are treatments available overseas to slow degeneration from the disease. Deborah Klyer from Fabry New Zealand spoke to Lisa Owen.
Topics
health