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Folliculotropic mycosis fungoides can affect the central nervous system in advanced stages.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

A woman with scalp lymphoma and hair loss improved with radiotherapy, highlighting the need for biopsies in similar cases.

A young man with an unusual type of scarring hair loss suggests a possible new variant of a known scalp condition.

A man with scalp and neck skin issues improved after a year of oral isotretinoin.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

Researchers created a new mouse model for studying scleroderma.

An 86-year-old man had a rare tongue melanoma but refused treatment, showing the need for early cancer detection and treatment.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

New mutations in the DSG4 gene cause a rare hair condition.

A specific mutation known for causing cancer is also found to cause a skin condition in a young girl.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

A girl with citrullinemia developed pili torti, suggesting a link between the hair condition and the metabolic disorder.

Mice with alopecia areata had wider lymphatic vessels in their skin.

The nodule was a benign cutaneous lymphadenoma, not cancer, and was successfully removed.

Deleting a specific protein in skin cells disrupts normal hair growth and development.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

Lichen planopilaris causes permanent hair loss and scarring due to damage to hair follicles and can be mistaken for other hair loss conditions.

Dermoscopy is useful for diagnosing lichen planopilaris and certain features may relate to disease duration, age, and gender.

Moth-eaten hair loss can be a sign of syphilis.

Wearing a wig caused a skin condition to develop in a woman with hair loss.

A genetic mutation in the LIPH gene causes hair loss and growth defects.

Lgr5 and the vitamin D receptor are key in controlling skin inflammation and tumor risk in mice.

A rare type of skin cancer on the scalp can be mistaken for hair loss, causing delayed diagnosis and severe damage.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

Some patients with a type of skin lymphoma can experience a rare, non-scarring hair loss that looks like another hair loss condition but has distinct features.

Lichen planopilaris in men often affects the scalp, eyebrows, arms, legs, and beard, with many having family members with hair loss.

GLI2 activates GLI1, promoting skin tumor growth and hair development.