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  • Hypophosphatasia (HPP) Symptoms, Causes Treatment
    Hypophosphatasia (HPP) is a rare genetic condition that softens your bones and can cause you to lose your teeth earlier than usual It has seven major forms that range in severity and age of onset
  • Hypophosphatasia | About the Disease | GARD - Genetic and Rare Diseases . . .
    Hypophosphatasia is an inherited disorder that affects the development of bones and teeth This condition disrupts a process called mineralization, in which minerals such as calcium and phosphorus are deposited in developing bones and teeth
  • Hypophosphatasia - Wikipedia
    Hypophosphatasia is a rare disease that has been reported worldwide and appears to affect individuals of all ethnicities [3] The prevalence of severe hypophosphatasia is estimated to be 1:100,000 in a population of largely Anglo-Saxon origin
  • Hypophosphatasia: MedlinePlus Genetics
    Hypophosphatasia is an inherited disorder that affects the development of bones and teeth This condition disrupts a process called mineralization, in which minerals such as calcium and phosphorus are deposited in developing bones and teeth
  • Hypophosphatasia (HPP) - Childrens Hospital of Philadelphia
    Hypophosphatasia, sometime shortened to HPP, is a rare inherited disorder that affects the development of bones and teeth In children and adults with hypophosphatasia, the bones and teeth do not absorb enough calcium and phosphorus
  • Hypophosphatasia - Symptoms, Causes, Treatment | NORD
    Hypophosphatasia (HPP) is a rare genetic disorder characterized by impaired mineralization (“calcification”) of bones and teeth Problems occur because mineralization is the process by which bones and teeth take up calcium and phosphorus required for proper hardness and strength
  • Hypophosphatasia | Home
    Learn about hypophosphatasia (HPP), its symptoms, and its effect on infants, children, and adults Find resources and tools to support your HPP journey
  • Soft Bones – Hypophosphatasia (HPP) Resources
    Hypophosphatasia (hī-pō-ˌfäs-fə-ˈtā-zh (ē-)ə) or HPP is an inherited (genetic) metabolic disorder People with this condition have low levels of the enzyme alkaline phosphatase (ALP), which often affects the development of bones and teeth


















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