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Folliculitis decalvans mainly affects middle-aged African American men and is treated with antibiotics.

Generalized trichoepitheliomas with hair loss may indicate myasthenia gravis.

Localized trichorrhexis nodosa is a hair condition where hair becomes fragile and breaks easily due to damage.

A rare benign tumor with hair follicle features was found on a man's trunk.

A rare skin bump with tiny hairs was successfully removed from a man's face.

The naked mutation in mice causes hair loss and helps identify keratin genes.

A girl had two rare hair conditions that helped understand their overlap.

A new technique effectively treats and diagnoses eruptive vellus hair cysts without recurrence.

The lump on a woman's scalp was a rare, potentially cancerous tumor from the hair follicle, not a common cyst.

Brodalumab is more effective than ustekinumab in treating psoriasis.

New technologies show potential for better understanding and treating skin conditions with abnormal mucin, but more research is needed for clinical use.

Trichogerminoma is a rare, benign skin tumor from hair cells, with a small risk of becoming cancerous.

Reticular erythematous mucinosis syndrome can occur with minimal mucin deposition.

An 11-month-old boy with Menkes disease had severe brain shrinkage and abnormal blood vessels, and didn't respond well to treatment.

Three dogs with a rare skin condition improved with treatment.

Isolated patchy heterochromia with pili annulati can occur without other health issues.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

Björnstad syndrome causes twisted hair from birth.

Dermoscopy can help diagnose tinea capitis in children by looking for comma hairs, black dots, and broken hairs with white bands.

A 32-year-old woman's hair loss was linked to skin nodules and severe headaches.

Cronkhite-Canada syndrome is a rare, non-inherited condition causing various symptoms like polyps, hair loss, and weight loss.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.

A 2-year-old girl had a hair disorder not shared by her identical twin.

A woman's hair loss was initially mistaken for a common hair loss condition but was later found to be caused by breast cancer cells in her scalp.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

The brothers have congenital ichthyosis, and the older brother's eye issues are due to different genetic mutations.

A woman had a non-cancerous skin tumor on her eyelid removed successfully.

Trichorrhexis nodosa is mainly caused by hair trauma and improves with gentler hair care.

SACUMAN, a rare condition causing hair loss without clear signs, is often misdiagnosed and needs scalp biopsies for accurate detection.

Cyclophosphamide likely causes skin darkening by affecting hair follicles.