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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
  • Resources - Galactosemia Foundation
    This galactosemia handbook presents current information for each life stage, including various symptoms that may appear Cited recommendations are based on the international clinical guideline, peer-reviewed data, expert insights, and first-hand experience from the galactosemia community
  • 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 - 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
  • 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
  • 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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