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Three Iranian men had reddish-brown facial pigmentation with no effective treatment.

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

TCHHL1 is a protein important for hair growth, found in hair follicles.

The hairless protein is important for skin, hair, and may influence cancer development.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

A trial showed that a new treatment is safe and effective for male pattern baldness, with most participants growing new hair.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

New therapies and trials are needed for Merkel cell carcinoma, a tough skin cancer.

Lichen planus pigmentosus may indicate undetected hepatitis C infection.

Taking Vitamin D supplements may increase the risk of skin darkening after laser hair removal.

Ovarian hyperthecosis can cause polycythemia, and surgery can normalize symptoms.

VR1 signaling can inhibit hair growth by affecting cell processes and increasing hair growth inhibitors.

The method effectively analyzes human hair proteins, especially nonfilamentous ones.

Skin changes and high vitamin B12 levels can be early signs of cancer.

Segmental vitiligo affects hair follicle melanocytes, causing small, uniform depigmented spots.

We need more research to better understand human hair follicle stem cells for improved treatments for hair loss and skin cancer.

A new gene mutation causes a rare type of hair loss.

A rare skin condition affected only the facial hair of a 46-year-old man.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

Intralesional cidofovir might be a good alternative treatment.

A man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

Sporadic trichoblastic neoplasms generally don't recur or spread, with one case showing a specific genetic fusion.

Gene variant linked to prostate cancer, hormone levels, and hair loss.

Keratoacanthomas and squamous cell carcinomas have similar keratin patterns, making them hard to tell apart.

PTCH gene mutations contribute to basal cell carcinoma development.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

A rare non-cancerous tumor that grows like hair was found in an unusual spot, the vulva.