Fragile X Syndrome: Experiences and Importance of Diagnosis
In this video four parents of individuals with Fragile X are interviewed about their experiences of receiving a diagnosis of Fragile X Syndrome. Professor Andrew Stanfield (Patrick Wild Centre) and Dr Margaretha Van Mourik (Clinical Geneticist) provide expert input. This video was funded by Awards for All, Big Lottery Scotland, as part of the project "Educate to Empower". Through this project the Fragile X Society and the Patrick Wild Centre trained professionals across Scotland about Fragile X Syndrome and produced a resource pack for newly diagnosed families.

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Family with Fragile X

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Adult Issues in Fragile X Syndrome

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Living w/ Fragile X | Studio 10

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Gendefekt Angelman: Wie Leveen trotzdem laufen lernt

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Living with Fragile X Syndrome: 'He is maturing ... it's just really slow' | USA TODAY

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La sindrome del cromosoma X fragile: la storia di Luca | The Real Italia

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Living with Fragile X

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A Kid with a Gene Mutation (Fragile X)

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My Life With Klinefelter's | Journey to Diagnosis

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Fragile X Society Conference 2022: Introduction; and Fragile X Premutation Associated Conditions

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Behind the Mystery Fragile X Syndrome: Genetic Disorder That Can Cause Learning/Behavior Challenges

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Der Fluch der Gewissheit - Alina kämpft gegen die Huntington-Krankheit | SWR Doku

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“Du simulierst doch nur!” - Kim hat Multiple Sklerose I einfach Mensch bei 37 Grad

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Fragile X - Hitting the Mark

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Fragile X-Associated Disorders: A Woman’s View from the Heart of the Family

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KSAT Community: Fragile X Awareness

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Fragile X syndrome | Genetics, cell biology and pathology of Fragile X syndrome | USMLE Step 1

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Fragile X Syndrome

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Introduction to Fragile X Syndrome

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