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

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

A woman with hypothyroidism stopped taking levothyroxine after successful homeopathic treatment.

The case shows the importance of quick and thorough evaluation of adrenal tumors to prevent rapid disease progression and poor outcomes.

Vitamin A toxicity likely caused the patient's high calcium levels.

Alkaline phosphatase activity decreases in early alopecia areata.

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.

A rare calcium deposit condition was found on a man's scalp.

Platelet-rich plasma treatment is effective for hair loss in patients regardless of their thyroid antibody levels.

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

Neuroendocrine paraneoplastic syndromes often show skin changes, helping early diagnosis and requiring a team approach for best care.

Early recognition of skin lesions in Birt-Hogg-Dubé syndrome is crucial for detecting renal tumors early.

Innate lymphoid cells type 1 may contribute to alopecia areata by damaging hair follicles.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

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

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps from birth.

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.

HLD10 can include increased body hair and Mongolian spots.

Thyroid hormone levels in children are linked to growth hormone and can be affected by diabetes in Riyadh, Saudi Arabia.

No effective treatment exists to stimulate hair growth in atrichia with papular lesions.

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Congenital atrichia with papular lesions causes permanent hair loss in children.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Different forms of the Vitamin D receptor can impact metabolic and hormone issues in Polycystic Ovary Syndrome.

A 15-year-old girl with missed periods was diagnosed with a pituitary disorder and treated with hormones and steroids.

A woman's masculine features were caused by a rare ovarian tumor that produced male hormones.

AHST shows promise for treating type 1 diabetes but needs more research before widespread use.

CRPS I is complex, linked to immune and nerve issues, and needs comprehensive treatment.