deficiency typeの例文
- These nonclassic forms of the disorder are sometimes diagnosed as familial glucocorticoid deficiency type 3.
- Lack of metabolically active aldosterone synthase leads to corticosterone methyl oxidase deficiency type I and II . The deficiency is characterized clinically by salt-wasting, failure to thrive, and growth retardation.
- In 2009, Monash Children's Hospital at Southern Health in Melbourne, Australia reported that a patient known as Baby Z became the first person to be successfully treated for molybdenum cofactor deficiency type A . The patient was treated with cPMP, a precursor of the molybdenum cofactor.
- "' Cyclic pyranopterin monophosphate "'( "'cPMP "') is an experimental treatment for molybdenum cofactor deficiency type A, which was developed by Jos?Santamar韆-Araujo and Guenter Schwarz at the German universities TU Braunschweig and the University of Cologne.
- Deficient aldosterone synthase activity results in impaired biosynthesis of aldosterone while corticosterone in the zona glomerulosa is excessively produced in both corticosterone methyl oxidase deficiency type I and II . The corticosterone methyl oxidase deficiencies both share this effect however type I causes an overall deficiency of 18-hydroxycorticosterone while type II overproduces it.