Adelantos recientes en genética molecular y presentación clínica de la deficiencia de 21-hidroxilasa
Salud(i)ciencia (Impresa); 15 (6), 2007
Congenital adrenal hyperplasia due to deficiency of the enzyme 21-hydroxylase (21-OH), is distinguished in its classical and nonclassical form and it is also one of the most common autosomal recessive inherited diseases in humans. The classical form appears in a rate between 1:5 000 and 1:15 000 among th...