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The virus linked to a rare disease was found in a patient's blood and urine before skin symptoms appeared.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

Trichodysplasia spinulosa is a rare skin disease in immunocompromised patients caused by a specific virus targeting hair follicle cells.

Antiviral medication valganciclovir may improve skin and hair in Trichodysplasia Spinulosa patients.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.

Trichodysplasia spinulosa is a rare skin condition caused by a virus, treatable with antiviral medication.

Leflunomide successfully treated a rare skin condition in a liver transplant patient.

Reducing immunosuppression and using antiviral creams improved the woman's skin condition.

Using cidofovir cream for a rare skin disease can cause skin darkening.

Topical tretinoin effectively treated sebaceous filaments, improving skin appearance.

Transplant patients often get skin problems, with treatments varying by condition.

A virus protein can activate a pathway that may lead to abnormal hair follicle development.

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

Oral valganciclovir improved a patient's skin condition caused by immunosuppression.

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

A rare case of a transplant patient developing a skin condition linked to HPV-49.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

New biopsy techniques and tools improve alopecia diagnosis, and both too much and too little selenium can cause hair loss.

Cilostazol may help hair grow and could be a new treatment for hair loss.

Certain microRNAs may protect against hair loss in alopecia areata and could be potential treatment targets.

Scientists can control how skin stem cells divide by using different treatments.

Dermal Wnt/β-catenin signaling is important for the proper size and development of hair follicles.

The protein CTCF is essential for skin development, maintaining hair follicles, and preventing inflammation.

Two boys developed a viral skin infection during chemotherapy, which resolved with improved immune function.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.