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

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Hair dyes and perms can damage hair and scalp, but using interventions can reduce harm.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

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.

Researchers found new hair and nail genes, how hair reacts to UV, differences in white and pigmented hair growth, nerve changes in alopecia, treatments for baldness and alopecia, a toenail condition linked to a genetic disorder, and that nail fungus is more common in people with psoriasis.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

Chemokine signaling is important for hair development.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

The conclusion is that teeth, hair, and claws have similar stem cell niches, which are important for growth and repair, and more research is needed on their regulation and potential markers.

Fungal infection was the main cause of hair loss in Egyptian children studied.

The document explains the genetic causes and characteristics of inherited hair disorders.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

Early treatment of children's hair loss, which can be caused by various factors, is important due to its emotional impact.

The document concludes that hair analysis is not good for assessing nutrition but can detect long-term heavy metal exposure.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

Hair changes can indicate systemic diseases or medication effects.

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

The document concludes that unruly hair can be congenital or acquired, often lacks specific treatments, and can be managed with oils and short hairstyles.

Loose anagen hair syndrome is caused by structural abnormalities in the hair follicle's inner root sheath.

Dlx3 is essential for hair growth and regeneration.

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

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