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

An 8-year-old girl had nail and hair issues that improved without specific treatment, but fungal nail infection was hard to cure.

Monilethrix is a rare, inherited condition causing fragile hair and hair loss, with no cure but some treatments may help.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

Accurate diagnosis is key for treating different kinds of hair loss, and immune response variations may affect the condition and treatment results.

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

A condition with certain scalp changes may come before acne keloidalis nuchae and other similar hair loss disorders.

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.

Finasteride and minoxidil are effective for hair regrowth, while treatments for alopecia areata have varying success and continuous treatment is necessary.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

About 30% of women feel they lose too much hair, often starting before age 40, and most can't find a reason for it.

Patients often experience long-lasting changes to their hair after stem cell transplants.

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

Hair ages due to various factors and treatments like minoxidil and finasteride can help, but more research and better public awareness are needed.

The conclusion is that an algorithm using trichoscopy helps diagnose different types of hair loss but may need updates and a biopsy if results are unclear.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Men with early hair loss may have a higher risk of enlarged prostate and possibly prostate cancer due to shared hormonal factors.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Male pattern hair loss is genetic and influenced by hormones, with treatments like minoxidil and surgery available.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Researchers found a gene mutation responsible for a rare hair loss condition.

Androgenic Alopecia, a common hair loss condition, can be effectively treated with finasteride and other treatments.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

Melatonin affects certain genes and pathways involved in cashmere goat hair growth.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

The WNT signaling pathway is important in many diseases and targeting it could offer new treatments.

Yellow and orange colors are important for diagnosing certain skin conditions.