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Trichoscopy is good for diagnosing and monitoring hair and scalp problems in children but needs more research for certain conditions.

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

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

RNA editing significantly affects hair growth and follicle cycling in the Tianzhu white yak.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Hair loss can cause significant social and emotional issues, especially for women and young men.

The 2015 Hair Research Congress concluded that stem cells, maraviroc, and simvastatin could potentially treat Alopecia Areata, topical minoxidil, finasteride, and steroids could treat Frontal Fibrosing Alopecia, and PTGDR2 antagonists could also treat alopecia. They also found that low-level light therapy could help with hair loss, a robotic device could assist in hair extraction, and nutrition could aid hair growth. They suggested that Alopecia Areata is an inflammatory disorder, not a single disease, indicating a need for personalized treatments.

Using methods like lasers and microneedling with drugs can improve hair regrowth for alopecia, but more research is needed on safety and best practices.

Fasting in hens affects thyroid hormones, which regulate feather and hair growth.

Tofacitinib helps regrow hair in severe alopecia patients, but more research is needed.

Light/laser therapy can effectively increase hair density in some types of alopecia, especially androgenic alopecia and alopecia areata.

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.

Understanding genetics is crucial for treating heart and skin diseases.

The document is a detailed medical reference on skin and genetic disorders.

Premature balding in some men may be linked to altered hormones, but it's not the male equivalent to polycystic ovary syndrome or metabolic syndrome.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

A new 3D culture system helps grow and study mouse skin stem cells for a long time.

Eyebrow loss has many causes and requires accurate diagnosis for proper treatment.

The document is a detailed guide on skin conditions and treatments for dermatologists.

Many patients at a dermatology clinic had scalp problems, often unrelated to why they visited, suggesting scalp checks should be regular.

A heart transplant patient developed a skin condition called epidermodysplasia verruciformis after taking immune-suppressing drugs.

Adalimumab significantly improves quality of life for patients with moderate to severe hidradenitis suppurativa.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

A woman was injured by a hedgehog falling on her, causing skin lesions but no disease.

LPA3 signaling in the uterus is crucial for placental formation and fetal development.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.