biotinidase deficiencies造句
例句与造句
- This is referred to as " late-onset " biotinidase deficiency.
- Biotinidase deficiency can also appear later in life.
- Profound biotinidase deficiency refers to situations where enzyme activity is 10 % or less.
- Individuals with partial biotinidase deficiency may have enzyme activity of 10-30 %.
- Approximately 100 mutations in the BTD gene that lead to biotinidase deficiency have been discovered.
- It's difficult to find biotinidase deficiencies in a sentence. 用biotinidase deficiencies造句挺难的
- The symptoms of biotinidase deficiency ( and dietary deficiency of biotin ) can be quite severe.
- There are at least 21 different mutations that have been found to lead to biotinidase deficiency.
- Symptoms are very similar to biotinidase deficiency and treatment large doses of biotin is also the same.
- Biotinidase deficiency is not due to inadequate biotin, but rather to a deficiency in the enzymes that process it.
- Neonatal screening for biotinidase deficiency began in the United States in 1984 and today many countries test for this disorder at birth.
- Because biocytin is the natural substrate of the enzyme biotinidase, biocytin can be used to measure the biotinidase activity and therefore diagnose biotinidase deficiency.
- They are for PKU ( phenylketonuria ), congenital hypothyroidism, congenital adrenal hyperplasia, biotinidase deficiency, maple syrup urine disease, galactosemia, homocystinuria and sickle cell anemia.
- _Biotinidase deficiency, occurring once in 70, 000 births, causing deficiency of the essential B vitamin biotin and resulting in frequent infections, uncoordinated movements, hearing loss, seizures and mental retardation.
- Almost all individuals with partial biotinidase deficiency ( 10-30 % enzyme activity ) have the mutation p . Asp444His in one allele of the " BTD " gene in combination with a second allele.
更多例句: 下一页