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Phenylketonuria - a long term condition - for iPad/Mac/PC

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Manage series 2306736
Content provided by The Open University. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by The Open University 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.
Phenylketonuria is an inherited long term condition where, from birth, the person is unable to break down an amino acid called phenylalanine, a component of proteins found in many common foods. If undiagnosed or untreated, the condition can disrupt normal brain development and lead to severe learning difficulties. There is no cure for PKU, but early diagnosis and a strict dietary regime allow both normal brain development and a full life span. In this collection, 18 year old Clair and 17 year old Jack share their knowledge and experience of living with PKU.
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5 episodes

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Manage series 2306736
Content provided by The Open University. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by The Open University 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.
Phenylketonuria is an inherited long term condition where, from birth, the person is unable to break down an amino acid called phenylalanine, a component of proteins found in many common foods. If undiagnosed or untreated, the condition can disrupt normal brain development and lead to severe learning difficulties. There is no cure for PKU, but early diagnosis and a strict dietary regime allow both normal brain development and a full life span. In this collection, 18 year old Clair and 17 year old Jack share their knowledge and experience of living with PKU.
  continue reading

5 episodes

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