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  • Galactosemia: Definition, Symptoms Treatment - Cleveland Clinic
    Galactosemia means “galactose in the blood” This inherited disorder prevents your body from breaking down the sugar galactose, causing it to build up to toxic levels in your blood People with galactosemia have to avoid dairy products, breast milk and most baby formulas
  • Galactosemia | About the Disease | GARD - Genetic and Rare Diseases . . .
    Galactosemia, which means 'galactose in the blood,' refers to a group of inherited disorders that impair the body's ability to process and produce energy from a sugar called galactose
  • Galactosemia - Wikipedia
    Galactosemia (British galactosaemia, from Greek γαλακτόζη + αίμα, meaning galactose + blood, accumulation of galactose in blood) is a rare genetic metabolic disorder that affects an individual's ability to metabolize the sugar galactose properly
  • Galactosemia: Symptoms, Causes, Diagnosis, Treatment - WebMD
    Galactosemia is a rare genetic condition that prevents babies from processing galactose, an important sugar in breast milk
  • Galactosemia - Symptoms, Causes, Treatment - NORD
    Learn about Galactosemia, including symptoms, causes, and treatments If you or a loved one is affected by this condition, visit NORD to find resources and
  • What is Galactosemia? | Galactosemia. com
    Learn about Galactosemia, including information on what this rare disease is, what causes it, who's affected by it, the types of Galactosemia, more
  • Galactosemia: MedlinePlus Genetics
    Researchers have identified several types of galactosemia These conditions are each caused by mutations in a particular gene and affect different enzymes involved in breaking down galactose Classic galactosemia, also known as type I, is the most common and most severe form of the condition
  • Types of Galactosemia - Galactosemia Foundation
    They are caused by a mutation or deletion in the GALT, GALK1, and GALE genes, the ones responsible for making the enzymes that are essential to metabolize galactose Classic galactosemia (type I) is the most severe form
  • Galactosemia - Causes, Symptoms, Diagnosis, and Treatment
    Galactosemia is a serious genetic disorder that requires early diagnosis and strict dietary management to prevent complications Understanding the condition, its symptoms, and treatment options is essential for individuals and families affected by galactosemia
  • Galactosemia: Biochemistry, Molecular Genetics, Newborn Screening, and . . .
    This review provides an overview of galactose metabolism, molecular genetics, newborn screening and therapy of galactosemia Novel treatments for galactosemia currently being investigated in (pre)clinical studies and potentially able to prevent long-term complications are also presented





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