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Nonclassic congenital adrenal hyperplasia
Current Opinion in Endocrinology, Diabetes & Obesity, 2012Late-onset or nonclassic congenital adrenal hyperplasia (NCAH) due to 21-hydroxylase deficiency is one of the most common autosomal recessive disorders. Reported prevalence ranges from 1 in 30 to 1 in 1000. Affected individuals typically present due to signs and symptoms of androgen excess.
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Congenital Virilizing Adrenal Hyperplasia
Archives of Pediatrics & Adolescent Medicine, 1960In the past several years, great strides have been made in the elucidation of certain inborn defects in steroid metabolism. This has led to a better understanding of the pathophysiology of congenital virilizing adrenal hyperplasia and has given us a more rational approach to the treatment of this disorder.
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Congenital adrenal hyperplasia
2007Congenital adrenal hyperplasia (CAH) is a group of disease characterized by deficencies of enzymes involved in synthesis of glucocorticoids, mineralocorticoids, and androgens. It is inherited in an autosomal recessive pattern. Steroids before blockade accumulate while those after blockade are produced in scanty amounts. There are six subtypes. The most
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