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FOXG1 Syndrome: Fighting the Odds

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Content provided by Dr Chris Smith and Will Tingle. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Dr Chris Smith and Will Tingle or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
Listener Vivek got in touch with a question about a rare genetic disease his son has, called FOXG1 Syndrone. In fact, it's so rare - and so newly-discovered - that only about six hundred people in the world have been diagnosed. Kids with FOXG1 have severe developmental delays; in Vivek's words, "everything that can go wrong - it's gone wrong with him." But the parents of FOXG1 children have been unusually tenacious when it comes to shaping the course of science. In this programme we meet those people blurring the line - metaphorically speaking - between the brain and the heart. Like this podcast? Please help us by supporting the Naked Scientists
  continue reading

102 episodes

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Fetch error

Hmmm there seems to be a problem fetching this series right now. Last successful fetch was on April 09, 2024 13:49 (17d ago)

What now? This series will be checked again in the next day. If you believe it should be working, please verify the publisher's feed link below is valid and includes actual episode links. You can contact support to request the feed be immediately fetched.

Manage episode 254078210 series 1335728
Content provided by Dr Chris Smith and Will Tingle. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Dr Chris Smith and Will Tingle or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
Listener Vivek got in touch with a question about a rare genetic disease his son has, called FOXG1 Syndrone. In fact, it's so rare - and so newly-discovered - that only about six hundred people in the world have been diagnosed. Kids with FOXG1 have severe developmental delays; in Vivek's words, "everything that can go wrong - it's gone wrong with him." But the parents of FOXG1 children have been unusually tenacious when it comes to shaping the course of science. In this programme we meet those people blurring the line - metaphorically speaking - between the brain and the heart. Like this podcast? Please help us by supporting the Naked Scientists
  continue reading

102 episodes

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