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Ultrasound is a useful, non-invasive tool in dermatology for diagnosing skin conditions and guiding treatments, but it has some limitations.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.

First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

A woman with long-term scalp psoriasis developed rare scarring hair loss that didn't fully respond to treatments.

Common types of non-scarring hair loss have various causes and treatments, but more effective solutions are needed.

A new side effect of aromatic retinoid treatment is soft nails.

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

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

A man with Acrodermatitis continua did not get better with etanercept treatment, and his condition worsened, suggesting treatment effectiveness may vary by genetics and race.

Primary health care in Florianópolis mostly treated simple skin conditions, while secondary care handled more complex skin diseases.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

The document concludes that stem cells and their environments are crucial for skin and hair health and have potential for medical treatments.

Anorexia Nervosa and Bulimia Nervosa are complex eating disorders with increasing incidence among young females, significant morbidity, and varying mortality rates, requiring more research for better treatment.

A new tool can analyze hair to detect changes due to hormones, genetics, and aging.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

Hair proteins in preschool children and their mothers could indicate developmental changes and health status.

COVID-19 reduced dermatology visits by 30.4%, with more male patients and increased cases of psoriasis, bullous diseases, and melanoma.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Alopecia areata is complex, often recurring, and needs personalized treatment, especially with other health issues.

Mothers have more hair proteins than their children, with age-related differences in protein patterns, and some proteins in hair could indicate early childhood development.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

Smoking and certain health conditions like thyroid disease may make palmoplantar pustulosis harder to treat.

Children with different rheumatologic diseases have specific skin symptoms that can help with diagnosis.

PDE inhibitors, especially PDE4 inhibitors like apremilast, are effective for certain inflammatory skin conditions but have side effects and can be costly.

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.

Certain gene variations might increase the risk of a hair loss condition in Koreans.

Experts discussed treatments for skin conditions in children, emphasizing hydration, cautious medication use, and early intervention for infections.