Search Results for: Prader Willi Syndrome

Patient Organization

Indian Prader Willi Syndrome Association

Patient Organization

International Prader Willi Syndrome Organization

NORD Rare Disease Report

Prader-Willi Syndrome

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Prader-Willi-like syndrome

NORD Rare Disease Report

Síndrome de Prader-Willi

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Prader-Willi syndrome

Sponsored Clinical Trial

Prader-Willi Syndrome

Patient Organization

Prader-Willi Syndrome Association (UK)

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Prader-Willi syndrome due to paternal 15q11q13 deletion

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Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15

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SIM1-related Prader-Willi-like syndrome

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Prader-Willi syndrome due to imprinting mutation

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Prader-Willi syndrome due to translocation

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Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2

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Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1

Patient Organization

International Prader-Willi Syndrome Organisation

Patient Organization

Prader-Willi Syndrome Association (USA)

Patient Organization

Foundation For Prader-Willi Research (FPWR)

Patient Organization

Prader-Willi France

News

Elisabeth Dykens, Ph.D.: 2018 Rare Impact Award Honoree

News

Five Years of Patient Registry Success: NORD’s IAMRARE™ Registry Program Celebrates New Partnerships and Models of Engagement

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Giving Spotlight: HomeServe USA Leadership and Employees Donate More Than $26,000 to NORD

NORD Rare Disease Report

Williams Syndrome

NORD Rare Disease Report

Síndrome de Williams

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Weaver-Williams syndrome

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