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WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

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

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

A gene mutation causes woolly hair in a Syrian patient.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

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.

Different hair loss types need accurate diagnosis for proper treatment.

Bimatoprost increases hair growth in mice without breaking down into other substances.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

Benzoyl peroxide and adapalene gels work differently to reduce acne in mice.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

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

Sonic hedgehog signaling is crucial for hair growth and maintaining hair follicle identity.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Aconiti Ciliare Tuber extract may help hair grow by activating a specific cell signaling pathway.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

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

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

Retinoids can prevent skin cancer in high-risk people but have side effects and require more research on dosing and effectiveness.

Certain genes are more active in baby scalp cells and can help grow hair when added to adult mouse skin cells.

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

t-Flavanone helps improve male pattern hair loss by making hair roots stronger.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.