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  2. Congenital adrenal hyperplasia - Wikipedia

    en.wikipedia.org/wiki/Congenital_adrenal_hyperplasia

    Young women may present with symptoms of polycystic ovarian syndrome (oligomenorrhea, polycystic ovaries, hirsutism). [medical citation needed] Males with classic CAH generally have no signs of CAH at birth. Some may present with hyperpigmentation, due to co-secretion with melanocyte-stimulating hormone, and possible penile enlargement.

  3. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency

    en.wikipedia.org/wiki/Congenital_adrenal...

    It is unclear what concentration of adrenal androgens is best for normal growth, puberty, and bone health. [221] One of the challenging aspects of long-term management is optimizing growth so that a child with CAH achieves his or her height potential because both undertreatment and overtreatment can reduce growth or the remaining time for growth.

  4. Hyperandrogenism - Wikipedia

    en.wikipedia.org/wiki/Hyperandrogenism

    Hyperandrogenism is a medical condition characterized by high levels of androgens.It is more common in women than men. [4] Symptoms of hyperandrogenism may include acne, seborrhea, hair loss on the scalp, increased body or facial hair, and infrequent or absent menstruation.

  5. Congenital adrenal hyperplasia due to 17α-hydroxylase ...

    en.wikipedia.org/wiki/Congenital_adrenal...

    Congenital adrenal hyperplasia due to 17α-hydroxylase deficiency is an uncommon form of congenital adrenal hyperplasia (CAH) resulting from a mutation in the gene CYP17A1, which produces the enzyme 17α-hydroxylase. [1] [2] It causes decreased synthesis of cortisol and sex hormones, with resulting increase in mineralocorticoid production.

  6. Congenital adrenal hyperplasia due to 11β-hydroxylase ...

    en.wikipedia.org/wiki/Congenital_adrenal...

    Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency is a form of congenital adrenal hyperplasia (CAH) which produces a higher than normal amount of androgen, [1] resulting from a defect in the gene encoding the enzyme steroid 11β-hydroxylase (11β-OH) which mediates the final step of cortisol synthesis in the adrenal. 11β-OH CAH results in hypertension due to excessive ...

  7. Androgen - Wikipedia

    en.wikipedia.org/wiki/Androgen

    Androgens are synthesized in the testes, the ovaries, and the adrenal glands. Androgens increase in both males and females during puberty. [3] The major androgen in males is testosterone. [4] Dihydrotestosterone (DHT) and androstenedione are of equal importance in male development. [4] DHT in utero causes differentiation of the penis, scrotum ...

  8. Lipoid congenital adrenal hyperplasia - Wikipedia

    en.wikipedia.org/wiki/Lipoid_congenital_adrenal...

    Ovarian and adrenal androgen production is minimal and produces little pubic or other body hair. [citation needed] However insufficient estradiol and progesterone are produced to induce maturation of an egg and ovulation. Although prepubertal ovaries are inactive enough that no lipid accumulates to cause damage, once they have begun to produce ...

  9. Achard–Thiers syndrome - Wikipedia

    en.wikipedia.org/wiki/Achard–Thiers_syndrome

    Symptoms: Diabetes mellitus, deep voice, hirsutism, clitoral hypertrophy, adrenal cortical hyperplasia or adenoma amenorrhoea, hypertension and osteoporosis. [1] Usual onset: Post menopausal. [2] Diagnostic method: Clinical findings. [2] Differential diagnosis: Acquired adrenogenital syndrome, empty sella syndrome, diabetes, and polycystic ...