Search

everythinglearnresearchcommunity

for

Search:↓

Some women with PCOS have CYP21 mutations and IRS1 variants, but these genetic factors are not major contributors to PCOS.

Women's ovarian hormones and adrenal androgens change throughout life, affecting hair loss and health.

These drugs cause hair growth without affecting testosterone or adrenal hormones.

Leydig cells can cause testosterone-secreting adrenal tumors in women.

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

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

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

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

Women with congenital adrenal hyperplasia have lower fertility, but with proper treatment, they can conceive successfully.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

A woman with a rare adrenal tumor and hormonal disorder had improved testosterone levels after surgery, but her menstrual irregularities continued.

Measuring 17-hydroxyprogesterone in hair can help monitor androgen levels in people with congenital adrenal hyperplasia.

Certain adrenal hormones can strongly stimulate oil gland growth in hamster skin, similar to male hormones.

Women with non-classical congenital adrenal hyperplasia have higher levels of certain steroids, which can be reduced by treatment.

Women with congenital adrenal hyperplasia (CAH) have more sexual function issues than those with polycystic ovary syndrome (PCOS), but physical activity can improve sexual functioning in all women.

Ashwagandha may improve hormone levels and reduce hair loss in non-classical adrenal hyperplasia.

Finasteride, when taken daily, lowers dihydrotestosterone levels but doesn't noticeably affect adrenal steroid production, except by blocking the 5 alpha-reductase enzyme.

Treating non-classic congenital adrenal hyperplasia is complex because the benefits of hormone treatment must be weighed against potential health risks.

GnRH analogue can help diagnose ovarian causes of high testosterone in postmenopausal women when scans don't show the cause.

Low DHEA-S levels might be linked to alopecia areata and could be a potential treatment target.

Some women with excess hair growth have a hormone condition that can't be diagnosed by blood or urine tests alone.

Natural products may help treat skin inflammation from abnormal adrenal hormones.

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

Goat hair shows changes in metal levels and stress when goats move from indoors to mountain pastures.

Diagnosing simple-virilizing congenital adrenal hyperplasia can be difficult and requires thorough testing and expert advice.

A woman developed Cushing syndrome and adrenal insufficiency from using fluticasone and ritonavir together.

Higher androgen levels during puberty are linked to shorter adult height in boys with Silver-Russell syndrome.

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 man's health improved after treating his undiagnosed adrenal insufficiency, which caused fatigue and weight loss.

Most dogs with adrenal-dependent hypercortisolism had normal blood pressure after one year of treatment or surgery.