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A 20-year-old woman was found to have a rare ovarian tumor causing symptoms like acne and a low-pitched voice, which disappeared after the tumor was removed.

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.

Alopecia neoplastica is hair loss from breast cancer spreading to the scalp.

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

Block and replace therapy improved symptoms in recurrent cyclic Cushing’s disease.

The ferret had a malignant apocrine gland tumor and did not survive surgery.

A Shi Tzu dog with high cortisol levels improved after increasing the dose of trilostane.

Adrenarche increases adrenal androgens around age 6, affecting hair growth and development.

Early diagnosis and treatment with corticosteroids can improve outcomes in Cronkhite–Canada syndrome.

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

Thymoma in cats can cause hair loss without inflammation.

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

A 22-year-old woman with a rare genetic condition was successfully treated to develop normal female characteristics and regular menstruation.

A 36-year-old woman with low potassium levels was found to have Cushing disease, and after treatment, her potassium levels normalized.

Removing the ovarian tumor improved the woman's hormonal symptoms.

A new gene variant causes glucocorticoid resistance in a mother and son.

Rare ovarian tumors can cause increased male hormones in postmenopausal women; surgery is an effective treatment.

Trilostane helped a cat with a hormone issue but the cat later died from a kidney infection.

A postmenopausal woman had rare symptoms due to a possible ovarian tumor, needing thorough evaluation.

A 13-year-old boy with Cushing syndrome has high cortisol levels from a pituitary gland issue and underdeveloped sexual characteristics.

Careful dosing and monitoring are crucial to prevent adrenal insufficiency when using ketoconazole for Cushing's disease.

Oestrogen does not affect adrenal androgen levels in children and adolescents.

A patient with Cronkhite-Canada Syndrome developed colon cancer that spread to the liver, showing the need for regular cancer checks in such patients.

A rare ovarian tumor can occur without causing male-like symptoms.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Corticosteroids improved symptoms in a man with Cronkhite-Canada Syndrome.