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Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Normal hair thickness varies by scalp area and a mix of hair thicknesses is typical in healthy individuals.

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

Hair examination helps diagnose rare neurological diseases in children.

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.

Minoxidil can improve hair growth in some patients with woolly hair due to LIPH variants, with varying responses and mild side effects.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

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

Temporal triangular alopecia is a non-scarring hair loss in children, often linked to other health conditions.

Fat tissue stem cells may help increase hair growth.

Growth factors and microneedle therapy increase hair density in women with hair loss.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

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

A woman developed rare, unexplained curly hair on her scalp and eyelashes.

A Korean girl developed kinky hair without known cause or effective treatment.

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

Trichoscopy is a quick, cost-effective tool for diagnosing different hair loss conditions.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

The document concludes that using specific tools and tests is essential for identifying the cause of hair loss and deciding on the right treatment.

The document concludes that understanding hair follicles requires more research using computational methods and an integrative approach, considering the current limitations in hair treatment products.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

Minoxidil, applied on the skin or taken orally, can improve hair growth in kids, but more research is needed due to possible side effects.

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

Selective breeding caused the unique curly hair in Mangalitza pigs.

Gintonin-enriched fraction promotes hair growth and could be a potential alopecia treatment.

Loose Anagen Hair Syndrome is found in black-haired Indian children and is often missed, especially in boys.

Using special RNA to target a mutant gene fixed hair problems in mice.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.