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Innhold levert av Andrew Hattersley and Maggie Shepherd, Andrew Hattersley, and Maggie Shepherd. Alt podcastinnhold, inkludert episoder, grafikk og podcastbeskrivelser, lastes opp og leveres direkte av Andrew Hattersley and Maggie Shepherd, Andrew Hattersley, and Maggie Shepherd eller deres podcastplattformpartner. Hvis du tror at noen bruker det opphavsrettsbeskyttede verket ditt uten din tillatelse, kan du følge prosessen skissert her https://no.player.fm/legal.
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Series 3 episode 8. HNF1Beta syndrome: kidney disease, diabetes, liver dysfunction and much more

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Innhold levert av Andrew Hattersley and Maggie Shepherd, Andrew Hattersley, and Maggie Shepherd. Alt podcastinnhold, inkludert episoder, grafikk og podcastbeskrivelser, lastes opp og leveres direkte av Andrew Hattersley and Maggie Shepherd, Andrew Hattersley, and Maggie Shepherd eller deres podcastplattformpartner. Hvis du tror at noen bruker det opphavsrettsbeskyttede verket ditt uten din tillatelse, kan du følge prosessen skissert her https://no.player.fm/legal.

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Grant King talks about his diagnostic journey where his low birth weight, childhood kidney disease, diabetes, liver dysfunction and infertility were at 32 years finally recognised as all being due to a change in the HNF1Beta gene. Dr Coralie Bingham explains how her research during her PhD in Exeter led to HNF1Beta being established as the commonest cause of inherited kidney disease and all the key parts of the HNF1Beta syndrome being recognised.

  continue reading

31 episoder

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Manage episode 459785416 series 3528389
Innhold levert av Andrew Hattersley and Maggie Shepherd, Andrew Hattersley, and Maggie Shepherd. Alt podcastinnhold, inkludert episoder, grafikk og podcastbeskrivelser, lastes opp og leveres direkte av Andrew Hattersley and Maggie Shepherd, Andrew Hattersley, and Maggie Shepherd eller deres podcastplattformpartner. Hvis du tror at noen bruker det opphavsrettsbeskyttede verket ditt uten din tillatelse, kan du følge prosessen skissert her https://no.player.fm/legal.

Send us a text

Grant King talks about his diagnostic journey where his low birth weight, childhood kidney disease, diabetes, liver dysfunction and infertility were at 32 years finally recognised as all being due to a change in the HNF1Beta gene. Dr Coralie Bingham explains how her research during her PhD in Exeter led to HNF1Beta being established as the commonest cause of inherited kidney disease and all the key parts of the HNF1Beta syndrome being recognised.

  continue reading

31 episoder

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