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Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Hair dyes and perms can damage hair and scalp, but using interventions can reduce harm.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

The document concludes that individualized treatments for hair issues are effective, certain hair changes can indicate neurocutaneous diseases, specific lotions improve skin health, laser hair removal works but needs more study on long-term effects, men's cosmetics are diverse, peeling is effective but can have side effects, and facial pigmentation is often due to overactive skin cells.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

Chemokine signaling is important for hair development.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Fungal infection was the main cause of hair loss in Egyptian children studied.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

Loose Anagen Syndrome causes easy-to-pull, thin hair, mainly in young girls, and improves with age.

The document concludes that unruly hair can be congenital or acquired, often lacks specific treatments, and can be managed with oils and short hairstyles.

Loose anagen hair syndrome is caused by structural abnormalities in the hair follicle's inner root sheath.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

The guide explains how to diagnose and treat hair loss in dogs, covering causes and treatments, with some conditions lacking treatment options.

Some horses lose hair without inflammation or itching due to various conditions, and while mainly a cosmetic issue, diagnosis requires examination and biopsies, and breeding is not advised if it's hereditary.

New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Early baldness in men may indicate risks for obesity, metabolic syndrome, insulin resistance, and heart disease, similar to women with PCOS. Alopecia areata is often linked with autoimmune diseases and mental health issues. Certain hair disorders are due to genetic issues, and chemotherapy can cause hair loss through specific biological pathways. Iron deficiency's link to hair loss is still disputed.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

TTD hair brittleness is caused by multiple structural abnormalities.

Mice with human skin protein K8 had more skin problems and cancer.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Three dogs with a rare skin condition improved with treatment.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

Adding cetirizine to minoxidil improves hair growth and thickness in women with androgenetic alopecia.