Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency

With glucocorticoid and mineralocorticoid replacement, these girls will reach the age of puberty. Because the ovaries are relatively inactive in fetal life and childhood, they sustain little damage from lipid accumulation during childhood. In the case of lipoid CAH due to StAR deficiency, when rising gonadotropin levels initiate puberty , despite the inefficiency of sex steroid synthesis, the ovaries will usually make enough estradiol to produce breast development, and in some cases even menarche , with menses continuing for some years. Ovarian and adrenal androgen production is minimal and produces little pubic or other body hair.

Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency

congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency

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congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiencycongenital adrenal hyperplasia due to steroid 21-hydroxylase deficiencycongenital adrenal hyperplasia due to steroid 21-hydroxylase deficiencycongenital adrenal hyperplasia due to steroid 21-hydroxylase deficiencycongenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency

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