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Hair loss increases between July and October, possibly due to UV light, and factors like skin type, hair color, and density may affect this. Dandruff can worsen hair loss conditions.

Increased Toll-like receptors in blood cells may contribute to alopecia areata and could be a target for new treatments.

Polish medical societies recommend personalized treatment for PCOS based on the patient's specific symptoms and use the Rotterdam criteria for diagnosis.

Rac1 is essential for proper hair structure and color.

A woman developed a persistent skin rash and hair loss from a condition linked to her increased L-tryptophan intake.

Long COVID affects over half of COVID-19 survivors, causing a range of symptoms like fatigue and neurological issues, with no specific treatment yet.

Some vitamins and minerals are important for preventing hair loss, but treating hair loss with them without a known deficiency is not proven effective.

Burn scars heal abnormally and more research is needed to find better treatments.

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

Psoriasis lesions have fewer and smaller oil glands, which might affect the condition's development.

Too much zinc in the diet can cause hair loss and color change in young mice by reducing copper in the body.

Low-dose oral minoxidil increases hair thickness and length in children with a hair disorder called Loose Anagen Hair Syndrome.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

M30 is a promising treatment for preventing hair loss during chemotherapy.

Knuckle Acanthosis Nigricans is common in Latin American youth and may indicate early insulin resistance, especially in those with normal weight.

A woman's ovarian tumor causing high testosterone was successfully removed, and her symptoms improved.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

The 14-3-3σ gene is essential for preventing hair loss.

α-parvin is necessary for skin and hair growth and for the correct orientation of skin cells.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Aquaporins could be new drug targets for treating polycystic ovary syndrome.

A rare autoimmune condition, Satoyoshi syndrome, can start in adults and improve with immunosuppressive treatment.

Blocking the mineralocorticoid receptor can help treat skin thinning caused by steroids.

The CUBIC protocol allows detailed 3D visualization of proteins in mouse skin biopsies.

Excessive hair growth is much more common in Chinese women with PCOS than in the general population.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

The stump-tailed macaque is a good model for studying human hair loss, but it's expensive and hard to find, while rodent models are promising for understanding hair growth and finding new treatments.

Testosterone undecanoate safely and effectively increased penis size in male children with 5-alpha-reductase deficiency.

Both classical and L-type atypical BSE from cattle can infect goats with different incubation times, and tests can distinguish between the two strains.

Alopecia areata may be caused by the immune system attacking hair follicles.