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    jeni Apr 11 2022 6:08 pm

    Welcome to the new oneMPSvoice platform. We hope that you will make yourself at home here.
    You will notice a lot of wonderful features here! We are especially excited about the Trusted Resources section, featuring hundreds of research studies, articles, and other information about mucopolysaccharidosis:
    https://www.onempsvoice.com/trusted-resources/

    See something of interest? Click on “Bookmark” for quick access later.
    The “rules of the ro…Read more

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    Nov 19 2020 12:10 pm

    Weak Bones1, Strong Wills: Stories of XLHRobert lives in Trucksville, PA. He was diagnosed with XLH at 6 years old through lab work. XLH runs on his mother’s side of the family. His mother, maternal grandmother, sister, and many aunts and cousins have all been diagnosed with XLH. However, his two sons do not have XLH.Robert wanted to share the following pain management tip: “Try to stay active and get out, out in the public. Don’t just sit …Read more

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    Nov 19 2020 12:10 pm

    Genetic Diagnosis of X-Linked Dominant Hypophosphatemic Rickets in a Cohort Study: Tubular Reabsorption of Phosphate and 1,25(OH)2D Serum Levels are Associated With PHEX Mutation TypeBackground:Genetic Hypophosphatemic Rickets (HR) is a group of diseases characterized by renal phosphate wasting with inappropriately low or normal 1,25-dihydroxyvitamin D3 (1,25(OH)2D) serum levels. The most common form of HR is X-linked dominant HR (XLHR) which is …Read more

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    Nov 19 2020 9:05 am

    From One Generation to the Next, Research Offers a World of OpportunityThose are the words Debbie Moore uses to describe her son Colton who, at 16 months of age, was diagnosed with a deforming bone disorder called X-linked hypophosphatemia (XLH). Both uncommon and painful, XLH causes rickets and osteomalacia, or softening of the bones. Patients are typically diagnosed during childhood and have bowed legs, short stature, and experience bone pain …Read more

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    Nov 17 2020 5:37 am

    https://www.onempsvoice.com/WebsiteContentSurvey123

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    Nov 17 2020 5:37 am

    https://www.onempsvoice.com/WebsiteContentSurvey123

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    Nov 17 2020 5:36 am

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    Nov 13 2020 12:46 pm

    Genetic Diagnosis of X-Linked Dominant Hypophosphatemic Rickets in a Cohort Study: Tubular Reabsorption of Phosphate and 1,25(OH)2D Serum Levels are Associated With PHEX Mutation TypeBackground:Genetic Hypophosphatemic Rickets (HR) is a group of diseases characterized by renal phosphate wasting with inappropriately low or normal 1,25-dihydroxyvitamin D3 (1,25(OH)2D) serum levels. The most common form of HR is X-linked dominant HR (XLHR) which is …Read more

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    Nov 13 2020 12:46 pm

    Genetic Diagnosis of X-Linked Dominant Hypophosphatemic Rickets in a Cohort Study: Tubular Reabsorption of Phosphate and 1,25(OH)2D Serum Levels are Associated With PHEX Mutation Type

    Background:
    Genetic Hypophosphatemic Rickets (HR) is a group of diseases characterized by renal phosphate wasting with inappropriately low or normal 1,25-dihydroxyvitamin D3 (1,25(OH)2D) serum levels. The most common form of HR is X-linked dominant HR (XLHR) which is

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    Nov 13 2020 12:46 pm

    Genetic Diagnosis of X-Linked Dominant Hypophosphatemic Rickets in a Cohort Study: Tubular Reabsorption of Phosphate and 1,25(OH)2D Serum Levels are Associated With PHEX Mutation Type

    Background:
    Genetic Hypophosphatemic Rickets (HR) is a group of diseases characterized by renal phosphate wasting with inappropriately low or normal 1,25-dihydroxyvitamin D3 (1,25(OH)2D) serum levels. The most common form of HR is X-linked dominant HR (XLHR) which is

    Read more

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