Article
Non-classical congenital adrenal hyperplasia.
Pediatric endocrinology reviews : PER - 1 Jan 2006
Dacou-Voutetakis Catherine, Dracopoulou Maria
Abstract excerpt
Deficiency of 21-hydroxylase constitutes the most frequent form of Congenital adrenal hyperplasia (CAH) and is classified into classical and nonclassical (NC) forms. The type of the molecular defect determines the severity of the phenotype with a high degree of concordance for the classical genot...
Topics
- Adolescent
- Adrenal Hyperplasia, Congenital
- Adult
- Child
- Female
- Genotype
- Glucocorticoids
- Humans
- Male
- Phenotype
- Point Mutation
- Pregnancy
- Steroid 21-Hydroxylase
