Home > D. General pathology > Genetic and developmental anomalies > Genetic metabolic diseases > non-classic 21-hydroxylase deficiency
non-classic 21-hydroxylase deficiency
Friday 12 June 2009
The non-classic 21-hydroxylase deficiency is a very common autosomal recessive disorder (1% incidence in parts of US), with mild cortisol deficiency, excessive adrenal androgens, no salt wasting. It is usually diagnosed by early adulthood.
See also
21-hydroxylase deficiency
congenital adrenal hyperplasia