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The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

Low iron levels may be linked to some types of hair loss in women.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Lichen planus is a skin condition that can resolve on its own, is linked to hepatitis C, and increases the risk of skin cancer.

Alopecia areata is a common autoimmune disease affecting about 2% of people, causing significant disability and often associated with mental health issues and other autoimmune conditions.

Lupus affects the body and skin, causing joint pain and skin issues that can be treated with steroids and antimalarial drugs.

Exosomes could potentially enhance tissue repair and regeneration with lower rejection risk and easier production than live cell therapies.

Lignans and neolignans from plants may help protect against various health issues, including cancer and heart disease.

The document concludes that molluscum contagiosum is a common, benign skin infection in children, often healing without scarring.

The document concludes that specific itchy skin diseases during pregnancy have varying fetal risks and treatments, including corticosteroids and other medications.

Fat tissue cells are a promising option for healing various diseases, but more research is needed to ensure they are safe and effective.

Hormones, especially androgens, play a key role in acne, which can be a symptom of systemic diseases like PCOS and may require targeted treatment.

Tissue-resident memory T cells can protect against infections and cancer but may also contribute to autoimmune diseases.

There are still challenges in diagnosing and treating chronic skin diseases, but there is hope for future improvements.

Researchers found 15 new genetic links to skin traits in Japanese women.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

FOXN1 gene variants cause low T cells and immune issues from birth.

A gene called HDAC9 might be a new factor in male-pattern baldness.

The drug enzalutamide may reduce the ability of the virus causing COVID-19 to enter lung cells.

The document concludes that future heart disease research should account for sex-specific differences to improve diagnosis, treatment, and outcomes.

Nude mice with grafted human skin developed scars similar to human hypertrophic scars.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Rosemary extracts with carnosic acid and carnosol can reduce the harmfulness of Staphylococcus aureus without stopping its growth.

The document suggests using standardized methods to track and measure hair loss in alopecia areata, including patient self-assessment and a 50% improvement in specific scores as a treatment goal.

Hair loss requires customized treatments based on its various causes and types.

Early diagnosis and treatment are crucial for preventing permanent hair loss in various scalp conditions, and while new treatments are promising, more research is needed to evaluate their effectiveness.

Behçet's Disease may be caused by genetic and environmental factors leading to abnormal immune responses, and stress management and new treatments could improve patient outcomes.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

Finasteride caused a rare skin rash in a man, which improved after stopping the medication.

Treg dysfunction is linked to various autoimmune skin diseases, and understanding Treg properties is key for new treatments.