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Ep. 58: New Hope in Fighting Duchenne Muscular Dystrophy

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Manage episode 401801882 series 3470035
Sisällön tarjoaa Nemours Children's Health. Nemours Children's Health tai sen podcast-alustan kumppani lataa ja toimittaa kaiken podcast-sisällön, mukaan lukien jaksot, grafiikat ja podcast-kuvaukset. Jos uskot jonkun käyttävän tekijänoikeudella suojattua teostasi ilman lupaasi, voit seurata tässä https://fi.player.fm/legal kuvattua prosessia.

Muscular dystrophy is a genetic disorder that makes the muscles of the bodies of those affected get weaker over time. There's no known cure, but there are treatments, and researchers continue to learn more about how to prevent and treat it.
In this episode, we discuss one specific type of genetic disorder: Duchenne muscular dystrophy, and learn about a new FDA-approved gene therapy that is bringing hope to families.
Learn More
Guests:
Omer Abdul Hamid, MD, Neuromuscular Neurologist, Nemours Children’s Hospital, Florida
Rulla Starr, Neuromuscular Program Coordinator, Nemours Children's Hospital, Florida
Host/Producer: Carol Vassar

Thanks for tuning in today! Please visit NemoursWellBeyond.org to catch all our episodes and sign up for our monthly newsletter. You can also use the voicemail feature on the website to leave a message with your episode ideas or questions — you just might be featured on an upcoming episode of the show.

Views expressed by guests do not necessarily reflect the views of the host or management.
Subscribe, review or let your voice be heard at NemoursWellBeyond.org.

  continue reading

86 jaksoa

Artwork
iconJaa
 
Manage episode 401801882 series 3470035
Sisällön tarjoaa Nemours Children's Health. Nemours Children's Health tai sen podcast-alustan kumppani lataa ja toimittaa kaiken podcast-sisällön, mukaan lukien jaksot, grafiikat ja podcast-kuvaukset. Jos uskot jonkun käyttävän tekijänoikeudella suojattua teostasi ilman lupaasi, voit seurata tässä https://fi.player.fm/legal kuvattua prosessia.

Muscular dystrophy is a genetic disorder that makes the muscles of the bodies of those affected get weaker over time. There's no known cure, but there are treatments, and researchers continue to learn more about how to prevent and treat it.
In this episode, we discuss one specific type of genetic disorder: Duchenne muscular dystrophy, and learn about a new FDA-approved gene therapy that is bringing hope to families.
Learn More
Guests:
Omer Abdul Hamid, MD, Neuromuscular Neurologist, Nemours Children’s Hospital, Florida
Rulla Starr, Neuromuscular Program Coordinator, Nemours Children's Hospital, Florida
Host/Producer: Carol Vassar

Thanks for tuning in today! Please visit NemoursWellBeyond.org to catch all our episodes and sign up for our monthly newsletter. You can also use the voicemail feature on the website to leave a message with your episode ideas or questions — you just might be featured on an upcoming episode of the show.

Views expressed by guests do not necessarily reflect the views of the host or management.
Subscribe, review or let your voice be heard at NemoursWellBeyond.org.

  continue reading

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