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A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Trichoscopy is a useful non-invasive method for diagnosing different hair loss conditions.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

Certain signals and genes play a key role in hair growth and regeneration, and understanding these could lead to new treatments for skin regeneration.

Wnt, Eda, and Shh pathways are crucial for different stages of sweat gland development in mice.

HIV can cause various severe or unusual skin conditions that help indicate the presence and stage of the disease.

The guide explains how to identify and treat children's hair loss, including fungal infections, autoimmune disorders, hairstyle changes, self-correcting conditions, and behavioral therapy for hair-pulling.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Hormone imbalances can cause specific skin changes, which may help in early detection of endocrine disorders.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

A 5-year-old boy's skin condition improved with systemic valganciclovir after a cardiac transplant and immunosuppressive therapy.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

The study concludes that the EDA2R gene is activated by p53 during chemotherapy but is not necessary for chemotherapy-induced hair loss.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

Different types of dog hair loss are linked to problems starting the hair growth phase and early hair cycle ending.

Hair-thread Tourniquet Syndrome, where hair or thread tightly wraps around a body part, is not rare and requires early detection to prevent serious damage.

Male faces age with more wrinkles and hair loss, influenced by both body changes and environmental factors.

Loose Anagen Syndrome causes easy-to-pull, thin hair, mainly in young girls, and improves with age.

Low-level laser therapy seems to help dogs with noninflammatory alopecia grow hair back.

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

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

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Leg hair can be used for eyelash transplants, resulting in fuller lashes with less maintenance.

Testosterone therapy improved physical and social health in a male with 49,XXXXY syndrome.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Hair loss has many causes and treatments, and losing some hair daily is normal; proper diagnosis is key, and minoxidil can help treat it.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.