DHPS FOUNDATION

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Leading the way in DHPS Deficiency Disorder research and education in order to find treatment, and a cure #curedhps #raredisease

Founded

2018

Facebook

52

X (Twitter)

46

Address

RESTON

Address: 12030 SUNRISE VALLEY DRIVE 450, RESTONWeb: Sign in to see organisation websiteFacebook: curedhpsX (Twitter): CureDHPSVolunteers: 5Revenue: 235000ICO: 824444634

Home Our genetics make us unique our struggles and triumphs unite us. Our Mission Identify Assist Treat Our mission is to help identify and assist individuals with rare genetic disorders and to work with interested researchers to develop treatment options and cures for those disorders. Our initial focus is on increasing awareness and understanding of patients with DHPS deficiencies and evaluating potential treatments to address those deficiencies. DHPS in the News Recessive Rare Variants in Deoxyhypusine Synthase an Enzyme Involved in the Synthesis of Hypusine Are Associated with a Neurodevelopmental Disorder IBRI Collaboration Helps Discover a New Genetic Disease 1 IN 10 AMERICANS ARE AFFECTED BY A RARE DISEASE 30 MILLION PEOPLE IN THE US ARE AFFECTED BY A RARE DISEASE 350 MILLION PEOPLE GLOBALLY ARE AFFECTED BY A RARE DISEASE OVER 7000 DISTINCT RARE DISEASES EXIST APPROXIMATELY 80 OF RARE DISEASES ARE CAUSED BY FAULTY GENES 50 OF PEOPLE AFFECTED BY RARE DISEASES ARE CHILDREN MAKING RARE DISEASES ONE OF THE MOST DEADLY AND DEBILITATING FOR CHILDREN WORLDWIDE ACCORDING TO THE NATIONAL HEALTH INSTITUTE.

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Paul

πŸ’š Thank you, DHPS Foundation, for your tireless efforts to raise awareness and support those affected by rare genetic disorders. Together, we can make a difference! #curedhps #raredisease

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Daniel

What are some effective strategies for raising awareness about DHPS deficiencies and engaging communities to support research efforts?

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Emil

🌟 It's inspiring to see organizations like DHPS Foundation leading the charge in research and education! Let’s unite for those impacted by DHPS deficiency and work towards a brighter future. #curedhps #raredisease

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Rachel

How can we better support families navigating the emotional and logistical challenges of rare genetic disorders like DHPS deficiency?

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RESTON

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