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New hair regrowth model introduced, imiquimod kills skin cancer cells, T-cadherin loss makes skin cancer more invasive, no strong link between PTCH1 gene and skin cancer after transplant, and male teens more likely to have hereditary hair loss.

A rare case shows alopecia areata and ITP occurring together, needing more research.

Trichilemmal carcinoma shares genetic changes with other skin cancers, suggesting similar causes and potential treatments.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Using thigh skin, doctors successfully rebuilt a woman's scalp after removing a large tumor, with no tumor return after 8 months.

Macular alopecia is a distinct, non-scarring hair loss pattern that mostly affects young Hispanic/Latinx females and often resolves on its own.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Early diagnosis and treatment of nail and skin conditions can improve health and appearance.

A baby with a skin condition improved with treatment but developed a rare form of the condition affecting only his trunk.

In Freixo de Espada à Cinta, many people have skin lesions, especially moles and acne.

A 7-year-old girl had unusually long eyelashes with no known cause or related health issues.

Repigmentation in vitiligo may come from melanocyte stem cells in the skin.

Mice with a mutated Dsg3 gene showed severe symptoms but not the typical blistering of pemphigus vulgaris.

New treatments and early diagnosis methods for permanent hair loss due to scar tissue are important for managing its psychological effects.

A 5-year-old boy's skin condition improved with systemic valganciclovir after a cardiac transplant and immunosuppressive therapy.

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

Alopecia areata and vitiligo can coexist, respond well to treatment, and may have a better prognosis together.

The silver marmoset's skin is thin, lacks pigment cells, and has unique features like keratinized spines and specialized glands.

A fungal skin infection was successfully treated with medication and compression therapy.

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

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

A woman developed a skin condition called Pemphigus Vulgaris after a treatment to help with hair loss.

Long-term use of minoxidil may cause hair follicles to transform into noticeable terminal hairs, leading to trichostasis spinulosa.

A Laotian man with unusual skin changes and multiple growths in his gut was diagnosed with Cronkhite-Canada Syndrome and improved with nutritional and immune-based treatments.

A 4-year-old girl has a rare hair condition causing fragile, short hair.

Consider TFI in facial hypopigmentation diagnoses and confirm with a biopsy.

A cat with a rare pancreatic tumor and diabetes died despite treatment, showing similar symptoms to a human condition.

Tacalcitol ointment effectively improves bilateral nevus comedonicus.