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Excluding alopecia and mucous membrane components from the CLASI-A score reduces its effectiveness in capturing important disease activity.

H19 boosts hair growth potential by activating Wnt signaling, possibly helping treat hair loss.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

Mechanical stimuli and CCL2 can help regenerate hair follicles in adult mice.

A patient with Cronkhite-Canada Syndrome developed colon cancer that spread to the liver, showing the need for regular cancer checks in such patients.

Keratin 19 helps identify skin stem cells, with its presence varying by body location, age, and culture stage.

Clascoterone is safe for the heart, even at high doses.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

The protein CCN2 controls hair growth by affecting hair follicle formation and stem cell activity in mice.

MM-CEP/NLCs could effectively treat lung inflammation.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

An elderly woman's upper lip lump, thought to be a mucocele, was actually a rare type of lymphoma usually found on legs, treated successfully with chemotherapy and radiation.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

Clouston syndrome can lead to skin cancer, so monitoring is crucial.

CCCA may involve the PD1/PDL1 pathway and increased caspase 3, leading to permanent hair loss.

Collagen XVII is important for cell functions and its absence can worsen cancer outcomes.

Targeting cholesterol, fatty acids, fibrosis, and mast cells may help treat CCCA.

Cronkhite-Canada syndrome is rare, has a poor prognosis, and requires early diagnosis and ongoing treatment.

Anti-CD19 therapy may help treat SLE and NMOSD.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

Cats likely have a reactive skin condition, while dogs may have a more complex, possibly cancerous one.

The CLASI is a reliable tool for measuring the severity of cutaneous lupus erythematosus.