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Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

The document concludes that understanding and managing hair loss in cancer patients is important, and more research is needed for better treatments.

Hair shaft disorders, often due to genetics or environment, lack specific treatments but can be managed with gentle hair care and may improve with age or topical treatments.

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.

Monilethrix causes fragile, patchy hair loss.

Accurate diagnosis and tailored treatments are crucial for managing hair loss in humans and animals.

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

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

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

Eyelashes are important for looks and eye protection, and more people are treating sparse eyelashes; more research is needed to understand eyelash biology and improve treatments.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Bimatoprost is a safe and effective treatment for making eyelashes longer, thicker, and darker.

Mutations in the KRT85 gene cause hair and nail problems.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

Disrupted stem cell signals in hairpoor mice cause hair loss.

The article suggests that hair transplant surgery may not be purely cosmetic because it treats a disease and calls for clearer guidelines on its classification.

A 5-year-old girl has sparse, dry, and brittle hair but is otherwise healthy.

The Hair India 2010 conference introduced a new hair loss classification and highlighted advanced diagnostic techniques in trichology.

Pregnancy can cause skin darkening, varicose veins, more sweating, hair growth, hair loss after birth, nail changes, and gum inflammation.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Bimatoprost, a glaucoma medication, may also help treat hair loss.

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.

Finasteride use linked to increased risk of sexual dysfunction, especially in younger people.

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

The research provides a gene-based framework for hair biology, highlighting the Hippo pathway's importance and suggesting links between hair disorders, cancer pathways, and the immune system.