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CD4+ skin cells may be precursors to basal cell carcinoma.

Muse cells keep their special features and can become different cell types even after being frozen and thawed three times.

Triple horizontal scalp biopsies are 98% accurate in diagnosing hair loss, better than single biopsies.

Children with systemic lupus erythematosus have different skin symptoms than adults.

A clinically suspected melanoma appeared benign under the microscope but was confirmed by specific tests and a rare mutation.

The document concludes that secondary syphilis cases are increasing and often misdiagnosed, pityriasis rubra pilaris can be distinguished from psoriasis by skin cell features, and different skin layers produce specific components during skin repair.

Cell death shapes skin stem cell environments, affecting inflammation, repair, and cancer.

Tofacitinib and adalimumab are promising treatments for cicatricial alopecia with few side effects.

Removing the outer skin layer increases drug absorption and offers non-invasive treatment options, with some methods allowing for quick skin recovery.

Recognizing unusual brain and skin symptoms is crucial for diagnosing lupus early.

A baby with maple syrup urine disease improved from skin problems by adjusting his diet to correct amino acid levels.

Blocking IL-17 can reduce skin inflammation in a mouse model of pityriasis rubra pilaris.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

An infant with a zinc deficiency skin disorder improved with zinc treatment.

A 22-year-old homosexual man was diagnosed with secondary syphilis, genital warts, and HIV, highlighting the high STI risk in men who have sex with men.

People with Down syndrome have a higher risk of skin disorders and need better screening and treatment.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The review emphasizes the need to recognize skin conditions that affect hair follicles and sweat glands to avoid misdiagnosis.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

A patient with a skin condition had unusual scarring hair loss but improved with treatment.

A one-year-old child with a genetic condition had symptoms improved by treating zinc deficiency.

Non-white organ transplant patients have worse skin cancer outcomes due to later diagnosis and treatment.

Centrosomes are essential for healthy skin and hair growth, and their role is different from that of cilia.

A woman with dermatomyositis improved after treatment for neck panniculitis, suggesting similar treatment for related conditions.

Polyunsaturated fatty acids, like arachidonic acid and eicosapentaenoic acid, can promote hair growth and may help treat hair loss.

Botulinum toxin type A significantly reduces scalp psoriasis severity compared to placebo.

The Polish Dermatological Society recommends personalized treatment for cutaneous lupus, including lifestyle changes, medications, and monitoring, with specific drugs for severe cases.

Cancer treatments targeting specific cells often cause skin, hair, and nail problems, affecting patients' lives and requiring careful management.

The document concludes that Cutaneous Lupus Erythematosus has different forms, is influenced by genetic and environmental factors, and can be treated with various medications, but more targeted therapies are needed.

Different connective tissue disorders have unique symptoms and treatments, with varying outcomes and often require ongoing care from a specialist.