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Triamcinolone acetonide therapy for hair loss may cause a skin condition called linear lichen planus.

The study found increased skin pigmentation and variable melanocyte density in a patient with Addison's disease.

The treatment improved hair color in most vitiligo patients without major side effects.

A rare skin growth in a baby was successfully removed without coming back.

The hamartoma is an abnormal hair growth with limited development in the upper hair follicle.

Some cancer treatments can cause abnormal fine hair growth.

A pilomatrixoma in the eyebrow can cause hair loss and skin lightening.

A rare skin disorder, nevus comedonicus, can appear on one side of the body following Blaschko's lines.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

Vogt–Koyanagi–Harada disease can cause rare hair growth on normally hairless thumb skin.

A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

Dermoscopy is useful for diagnosing Atrichia with Papular Lesions in children without needing a biopsy.

Two patients had a rare combination of red skin spots and white scaly skin lesions not on the genitals.

The newborn's skin condition improved over time, leaving only lighter skin patches.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

Laser treatments are the most effective for porokeratotic adnexal ostial nevus.

The patient showed signs of liver disease due to alcohol use but didn't need treatment for Dupuytren’s contracture.

Imatinib can cause hair loss due to lichen planopilaris.

A rare combination of halo nevi, nonsegmental vitiligo, and early gray hair can occur together.

Ectopic acanthosis nigricans can occur at surgical sites due to skin graft mismatches.

Aggressive SLE treatment helped hair regrowth and improved oral plaque, but scalp lesions stayed.

Topical treatment improved rare scalp lichen amyloidosis.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

A young man's cheek papule was identified as a benign hair follicle tumor using a skin surface microscope.

Most cases were lichen planus pigmentosus, highlighting the need for accurate diagnosis for proper treatment.

The man has a genetic skin condition called pachyonychia congenita.

Trichodysplasia spinulosa can occur after a heart transplant due to immunosuppressive drugs.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

Lichen planus pigmentosus and fibrosing frontal alopecia in Colombia are likely different stages of the same disease.