Search

everythinglearnresearchcommunity

for

Search:↓

Late diagnosis of congenital adrenal hyperplasia can greatly affect physical development, gender identity, and sexual health.

A woman's adrenal tumor disappeared after treatment with cyproterone acetate.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

Adrenal glands delay the start of winter fur growth in mink.

Sparse hairs below frontal hairline can indicate early male balding.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

Removing an adrenal tumor can significantly reduce high androgen levels in postmenopausal women.

Early balding in men is linked to metabolic syndrome, so screening is important for prevention.

About 2.2% of women with symptoms of high male hormones have a mild form of congenital adrenal hyperplasia, and measuring a specific hormone level can accurately diagnose it.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

Finasteride reduces hair loss and treats BPH without major hormone changes, but may cause sexual dysfunction.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Some men with early hair loss may have a male version of PCOS, affecting hormones and increasing health risks.

The study found no significant difference in stress hormone levels between people with alopecia areata and healthy individuals, suggesting that the disease is not caused by an overactive stress response system.

Women with a certain type of tumor had higher levels of pregnancy hormone and male hormones, which decreased after treatment.

A boy's hair loss improved after tumor removal and vitamin D treatment, but hair loss returned despite normal vitamin D and no tumor regrowth.

A thorough diagnostic process and teamwork are crucial for managing complex hyperandrogenism in postmenopausal women.

A patient produced cortisol after adrenalectomy, possibly due to residual tissue or other body parts making steroids.

Testing basal 17-HP levels is a good way to screen for nonclassic adrenal hyperplasia in women with high androgen levels.

Minoxidil promotes hair growth in male pattern baldness.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Women with early hair loss have higher blood pressure and aldosterone; screening and treatment may help.

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

Young men with early hair loss have slightly worse blood sugar and fat levels, suggesting possible health risks and need for monitoring.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

New hair loss treatments may include topical medications, injections, and improved transplant methods.

Smoking increases early hair loss risk in men; quitting may help prevent it.

Young girls whose mothers have PCOS may have higher activity of a specific enzyme that could lead to developing PCOS later.