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The TT/DHT ratio may help identify PCOS patients with severe metabolic issues.

Biotin improved hair growth and combability in one child with uncombable hair syndrome.

A rare ovarian tumor caused early puberty in a 3-year-old girl.

Ovarian hyperthecosis should be considered in young women with severe male-like symptoms and can be managed with hormone treatments.

Advanced microscopy shows hair damage and keratin proteins' roles, aiding future cosmetic treatments.

The document honored Yvonne, announced upcoming dermatology events, and introduced new journal editors.

Dermoscopy helped correctly diagnose a skin condition that was previously misidentified as a different hair loss disease.

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

Netherton's syndrome may have a familial link and doesn't always include atopy.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

A woman's mature cystic teratoma caused her virilization by producing testosterone.

The newborn with Klippel-Trénaunay syndrome was healthy but needed regular check-ups for possible complications.

Triptorelin helps evaluate hormone production in Sertoli-Leydig cell tumors.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

Stress may cause sudden hair whitening in children.

A man with Cronkhite-Canada syndrome improved significantly with immunosuppressive therapy.

Trichoscopy helped diagnose a teenage girl's hair loss as monilethrix.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Accurate diagnosis of progressive supranuclear palsy requires thorough neurological assessments and MRI.

A CCS patient with severe complications was successfully treated using combined therapies.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Non-classical 21-hydroxylase deficiency can be missed in newborn screenings and should be considered in cases of early puberty or virilization.

Untreated Sheehan's Syndrome caused severe heart failure in a woman, which improved with hormone and heart failure treatment.

Sheehan syndrome can cause hormone deficiencies after childbirth, but treatment can improve symptoms.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Tabby mutations in mice affect hair follicle development and help study genetic mapping and certain medical conditions.

A 6-year-old girl was diagnosed with a rare hair disorder called monilethrix.

Two patients treated with TAC for mouth fibrosis improved but developed Cushing's Syndrome symptoms.

A 12-year-old girl with very high testosterone and insulin resistance improved with birth control pills, suggesting PCOS can cause high testosterone without tumors.