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Chemotherapy can cause significant hair thinning and changes in hair texture, while tamoxifen has a smaller effect.

Trichoscopy is a useful tool for diagnosing hair and scalp diseases without needing skin biopsies.

The document explains hair and nail biology, common hair loss conditions and treatments, oral and genital skin diseases, and the risks and treatments associated with squamous cell carcinoma.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

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

Future hair cosmetics will be safer and more effective.

Afro-textured hair needs personalized care due to its unique genetic traits.

Certain gene variants can cause inherited hair diseases, which are important to diagnose and understand for patient care.

A gene mutation causes woolly hair in a Syrian patient.

A patient with a rare hair condition and skin disorder showed hair improvement after treatment.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

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.

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

VEGF helps squamous cell carcinoma grow in ways beyond just blood vessel formation.

Lysophospholipids like LPA and S1P are important for hair growth, immune responses, and vascular development, and could be targeted for treating diseases.

Lysophosphatidic acid is important for skin health and disease, and could be a target for new skin disorder treatments.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

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

Keratin proteins are increasingly recognized as important for cell health and are linked to many diseases.

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

Early hair loss in men and women may indicate a higher risk of heart disease and metabolic problems.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

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

Disrupted cholesterol production impairs hair follicle stem cells, leading to hair loss.

Some drugs can cause reversible hair loss, but certain chemotherapy drugs may lead to permanent hair loss; drugs can also change hair color and texture.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.