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A protein called ectodysplasin-A2 increases a hair growth inhibitor in balding cells, which could be a target for hair loss treatment.

CD2 might be a new treatment target for patchy alopecia areata.

Hydroxypinacolone retinoate is a potent anti-aging ingredient for skin that is more effective and less irritating than other forms of retinoids.

Twins had rare skin cysts likely due to genetics.

A patient with total hair loss developed vitiligo after using a treatment called DCP.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Topical PUVA and tacrolimus ointment can effectively and safely treat infant alopecia universalis.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

Early diagnosis is crucial for treating alopecia effectively.

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

Biotin supplements are unnecessary for most people but may help with certain conditions like biotin deficiency, brittle nails, and some hair loss.

Telogen Effluvium is a common hair loss condition, particularly in women, with no specific FDA-approved treatment, and recovery can take up to 18 months.

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

Skin patterns form through molecular signals and genetic factors, affecting healing and dermatology.

Mutation in hairless gene may increase hair loss risk.

NF-κB signaling is crucial in many diseases and can be targeted for new treatments.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

A Thai boy was diagnosed with a rare hair disorder causing hair thinning and shedding.

Fzd2 is important for skin and hair development through various signaling ways.

Telogen Effluvium is a common hair loss condition that can be short-term or long-lasting and is often caused by stress, illness, or nutritional issues.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

Understanding skin structure and development helps diagnose and treat skin disorders.

The document explains hair and nail biology, common hair loss conditions and treatments, oral and genital skin diseases, and the risks and treatments associated with squamous cell carcinoma.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

The meeting highlighted major advances in skin research, including new findings on skin microbes, genetic links to skin diseases, and improved treatments for various conditions.

Certain micronutrients may improve hair and nail health, but more research is needed to confirm their benefits.