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

AMH levels can't reliably tell the difference between LOCAH and all types of PCOS in women with excessive hair growth.

Neurosteroids play a key role in controlling the brain-adrenal gland activity in pregnant sheep, both in normal and stressful situations.

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

Recreational drug use can cause misdiagnosed conditions and drug interactions in HIV patients.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

Melatonin and cortisol affect mink winter hair growth, but β-endorphin levels do not.

Stopping steroids and providing supportive care improved the patient's Cushing Syndrome symptoms and ulcers.

DAVID syndrome is a condition with immune system and hormone deficiencies, needing early diagnosis to avoid serious complications.

New treatments for the autoimmune hair loss condition alopecia areata may include JAK inhibitors and other immunomodulators.

Melasma is a skin condition linked to female hormones, genetics, UV exposure, and certain medications, but not to pituitary, adrenal, or thyroid diseases.

Methyl prednisolone helps most patients with alopecia universalis regrow hair.

Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

The document concludes that proper diagnosis and individualized treatment are crucial for managing androgenization in women effectively.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

Women with excessive hair growth or polycystic ovary disease may more often carry a gene variant for 21 hydroxylase deficiency.

The desmopressin stimulation test helped identify an adrenal cause for a patient's Cushing's syndrome.

Treating classic 21-hydroxylase deficiency requires precise glucocorticoid dosing and attention to individual patient needs, with new treatments showing promise.

The patient likely has Chrousos syndrome, a rare condition causing insensitivity to glucocorticoids, requiring high-dose dexamethasone treatment.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

A woman's hair loss and other symptoms were due to a rare hormone deficiency treatable with steroids.

Stress hormone CRF causes hair loss and inhibits hair growth in human cells.

A patient with untreated congenital adrenal hyperplasia had large benign tumors in her adrenal glands removed, improving her symptoms.

Stress hormone CRF causes hair loss and stops hair cell growth.

Skin symptoms like fragile skin and easy bruising can indicate Cushing's syndrome, which requires early diagnosis and treatment to prevent serious health issues.

New treatments for alopecia areata, like JAK inhibitors and immunomodulators, are promising.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

Human scalp hair follicles can produce and respond to several hormones, affecting hair growth and pigmentation.

A woman with childhood growth hormone deficiency had multiple hormone deficiencies and developed serious lung and kidney problems later in life.

A Miniature Pinscher dog with hair loss and scaling was diagnosed with pattern alopecia and improved with melatonin treatment.