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Cyclosporin doesn't stop hair loss.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Edar signaling is crucial for proper hair follicle development and function.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

The author found the Dermatology Nurses’ Association’s annual meeting valuable for both learning and making friends.

Cicatricial alopecia, a permanent hair loss condition, is mainly caused by damage to specific hair follicle stem cells and abnormal immune responses, with gene regulator PPAR-y and lipid metabolism disorders playing significant roles.

Lactic acid cream can help improve skin bumps known as eruptive vellus hair cysts.

The 2004 hair research meeting presented new findings on hair cell differentiation, genetic factors in hair loss, hair pigmentation, and potential targeted therapies.

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.

Women experience various skin issues at different life stages, requiring careful treatment and awareness.

The document explains different types of skin lesions and their characteristics, causes, and related conditions.

The document concludes that understanding how the skin's immune system and inflammation work is complex and requires more research to improve treatments for skin diseases.

Men generally have more severe COVID-19 cases and higher death rates than women due to biological differences.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

A20 protein is crucial for normal skin and hair development.

Certain signals and genes play a key role in hair growth and regeneration, and understanding these could lead to new treatments for skin regeneration.

A new type of sudden, complete female hair loss was found, with most patients fully recovering within 6 months without needing steroid treatment.

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

Scarring alopecias are complex hair loss disorders that require early treatment to prevent permanent hair loss.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

Permanent hair loss from cicatricial alopecia is treated by reducing inflammation and managing symptoms, but regrowth in scarred areas is unlikely.

NF-κB is crucial for different stages and types of hair growth in mice.

Most skin diseases in Hajjah, Yemen, were dermatitis, infections, and acne, influenced by local socioeconomic and environmental factors.

The document concludes that hair loss is common and can be treated with medications like minoxidil or surgical options, and it significantly affects people's psychological well-being.

Most hospitalized children with skin issues were boys, with allergic skin diseases like atopic dermatitis being most common, and treatments were usually topical.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

The Korean study found that twenty-nail dystrophy mainly affects adults, more often women, and has five distinct types with different clinical progressions.