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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 - 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 | 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 When people with Galactosemia injest foods or liquids containing galactose, undigested sugars build up in the blood
  • Galactosemia: Symptoms, Causes, Diagnosis, Treatment - WebMD
    Galactosemia is a rare genetic condition that prevents babies from processing galactose, an important sugar in breast milk Though the disease can cause many issues, it’s easily diagnosed and
  • Classic Galactosemia and Clinical Variant Galactosemia
    The diagnosis of classic galactosemia and clinical variant galactosemia is established by detection of elevated erythrocyte galactose-1-phosphate concentration, reduced erythrocyte galactose-1-phosphate uridylyltransferase (GALT) enzyme activity, and or biallelic pathogenic variants in GALT
  • Galactosemia: Symptoms, Diet, Diagnosis, and More - Healthline
    Galactosemia is a rare genetic disorder that affects how your body metabolizes galactose Galactose is a simple sugar found in milk, cheese, yogurt, and other dairy products When
  • Galactosemia: Biochemistry, Molecular Genetics, Newborn Screening, and . . .
    Galactosemia is a rare inborn metabolic disorder of carbohydrate metabolism presenting with multi-organ involvement and is potentially fatal if not diagnosed on time Biochemically, it is characterized by hypergalactosemia, a condition associated with an increased blood level of galactose
  • Galactosemia: Causes, Symptoms, and Treatment Options - Medicover Hospitals
    Galactosemia is an inherited disorder caused by the deficiency of enzymes needed to convert galactose into glucose, the primary energy source for cells The inability to process galactose results in its accumulation in the blood, leading to a range of symptoms and potential complications
  • GALACTOSEMIA (GALACTOSE INTOLERANCE): CAUSES, SYMPTOMS, TREATMENT
    Galactosemia is an infrequently seen genetic disorder that can provoke serious health complications if left untreated A deficiency in one of the enzymes responsible for breaking down galactose causes it





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