Ep.#8 - 💜 Family Series: Brenda King - Molecular Testing at Age 33- Leanna's Story episode artwork

EPISODE · Aug 29, 2024 · 2H 30M

Ep.#8 - 💜 Family Series: Brenda King - Molecular Testing at Age 33- Leanna's Story

from CdLS Connections · host Canadian CdLS Foundation

Join us to hear the story of Leanna who has lived with the diagnosis of CdLS for over 30 years. Only last year at the age of 32 did Leanna receive molecular testing to find out that she did not have Cornelia de Lange Syndrome but another rare syndrome, Rubinstein-Taybe Syndromes (RTS). Join us in hearing discussion with Leanna's mom, Brenda King, as she shares the Leanna's journey and similarities and differences between CdLS and RTS. An example of the benefits of advancements in genetics and the importance of molecular testing.Send us Fan MailSupport the showThanks for listening to CdLS Connections brought to you by the Canadian CdLS Foundation.Stay connected with our community at www.canadiancdlsfoundation.com and follow us on social media for more stories, support and updates. Together, we're building awareness and connection for everyone affected by Cornelia de Lange Syndrome.(c) Canadian CdLS Foundation. All Rights Reserved.

Join us to hear the story of Leanna who has lived with the diagnosis of CdLS for over 30 years. Only last year at the age of 32 did Leanna receive molecular testing to find out that she did not have Cornelia de Lange Syndrome but another rare syndrome, Rubinstein-Taybe Syndromes (RTS). Join us in hearing discussion with Leanna's mom, Brenda King, as she shares the Leanna's journey and similarities and differences between CdLS and RTS. An example of the benefits of advancements in genetics and...

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Ep.#8 - 💜 Family Series: Brenda King - Molecular Testing at Age 33- Leanna's Story

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How long is this episode of CdLS Connections?

This episode is 2 hours and 30 minutes long.

When was this CdLS Connections episode published?

This episode was published on August 29, 2024.

What is this episode about?

Join us to hear the story of Leanna who has lived with the diagnosis of CdLS for over 30 years. Only last year at the age of 32 did Leanna receive molecular testing to find out that she did not have Cornelia de Lange Syndrome but another rare...

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