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The document concludes that hair loss is complex, affects many people, has limited treatments, and requires more research on its causes and psychological impact.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Aging reduces skin stem cell function, leading to changes like hair loss and slower wound healing.

Hair growth serums A and C can affect hair growth genes and pathways, suggesting potential for personalized hair loss treatments.

The document concludes that understanding hair follicle histology and the hair cycle is crucial for diagnosing alopecia.

Androgenetic alopecia is more common in Saudi men than women.

The patient likely has Chrousos syndrome, a rare condition causing insensitivity to glucocorticoids, requiring high-dose dexamethasone treatment.

The document concludes that the risk of sexual side effects from 5-alpha-reductase inhibitors is low and often temporary, but more research is needed on potential permanent effects.

Skin problems in the elderly are unique and may indicate other diseases, involving changes in skin, hair, nails, and increased cancer risk.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

Scalp melanoma is often diagnosed late in people with hair loss, leading to worse outcomes.

Male pattern hair loss may have evolved to promote younger fathers for offspring health and survival, encouraging monogamy and paternal nurturing.

Six new risk spots for early hair loss were found, which also link to Parkinson's disease and lower fertility. Two genes, FOXA2 and HDAC4, could be new treatment targets. Hair loss might also be connected to heart disease, metabolic syndrome, and prostate cancer.

Ultraviolet rays damage hair, smoking may cause hair loss, and good nutrition is important for hair health, but genetics mainly decide hair thickness.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

Skin aging reflects overall body aging and can indicate internal health conditions.

Hairless mammals evolved quickly in both gene and non-gene areas related to skin and hair.

TRPV3 could be a target for treating pain, skin disorders, and hair problems, but more research is needed to create effective drugs.

Early onset hair loss linked to genetics and androgen levels.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

Men with male pattern baldness have a higher risk of aggressive prostate cancer and benign prostatic hyperplasia.

Vertex baldness has higher DHT levels than frontal baldness, but testosterone and PSA levels are similar.

Baldness is common in Korean men (60.5%), and those with a family history are 3.1 times more likely to have hairline recession.

Male pattern baldness is linked to a higher risk of certain skin cancers, especially on the scalp.

The research found that PCOS has common genetic factors regardless of how it is diagnosed and is linked to metabolic and reproductive issues.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Men with male-pattern baldness have more androgen receptors in their scalp's oil glands, which may contribute to hair loss.