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The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

An elderly man's hair grew back after treatment with secukinumab, possibly due to reduced scalp inflammation or the medication's direct effects.

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.

C-scores can help predict gain-of-function and loss-of-function mutations.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

More research with diverse participants is needed to determine the effectiveness of photobiomodulation devices for hair loss treatment.

The created skin model with melanoblasts improves the study of skin color and offers an alternative to animal testing.

Testosterone affects androgen receptors and lipid storage in cells, while DHEA does not convert to testosterone or affect these receptors in the same way.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

New treatments targeting specific genes show promise for treating keratin disorders.

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

Docetaxel and paclitaxel for breast cancer can cause permanent, severe hair loss.

Special immune cells called Regulatory T cells help control skin inflammation and repair in various skin diseases.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

People with Down's syndrome often have more skin problems due to a weak immune system.

New treatments for advanced skin cancer are improving patient outcomes, but drug resistance and finding the right treatment combinations are still big challenges.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

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.

Current therapies cannot fully regenerate adult skin without scars; more research is needed for scar-free healing.

Using cetirizine on the skin and taking vitamin D can help increase hair growth in children with hair loss from ectodermal dysplasia.

Effective treatment for hidradenitis suppurativa varies, with antibiotics commonly used and surgery as an option, but no single method is universally successful.

People with alopecia areata often have thyroid autoimmunity.

Pangolins have lost some skin-related genes, but kept others, leading to their unique scales and skin features.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.

AP-2α and AP-2β proteins are essential for healthy adult skin and hair.