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A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Hair loss should be medically treated, as non-medical treatments are ineffective and hair loss can indicate serious health issues.

Most women with excess hair growth had Polycystic Ovary Syndrome, and severity wasn't linked to hormone levels.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Inhibitors of 11β-HSD1 show potential for treating type 2 diabetes but require more testing for safety and effectiveness.

The ABHRS is expanding globally and advancing hair restoration surgery.

HSA nanoparticles can improve tamoxifen delivery for breast cancer treatment, reducing side effects.

Nestin identifies specific progenitor cells in hair follicles that can become outer root sheath cells.

Niosomes are a promising, stable, and cost-effective drug delivery system with potential for improved targeting and safety.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

A woman with asthma improved from a severe fungal infection after treatment change, and most HIV-positive women in a UK study had low immune cell counts but were responding well to treatment.

Providing housing and case management reduces hospital visits for chronically ill homeless adults.

A woman's hair loss and other symptoms were due to a rare hormone deficiency treatable with steroids.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Hair follicle stem cells and their exosomes help repair nerve injuries.

Hair follicle stem cells and their exosomes help repair nerve injuries.

The hairless protein is important for skin, hair, and may influence cancer development.

The conclusion is that hirsutism is strongly linked to PCOS and higher levels of certain hormones, but not to DHEAS, prolactin, cortisol, or TSH.

SAHA syndrome is a condition in women involving skin and hair issues, often related to hormonal imbalances, and is treated based on the underlying cause.

A 14-year-old girl's black hair showed unique color changes, suggesting early greying.

Personalized homeopathic treatment improved chronic spontaneous urticaria symptoms.

Hes1 protein is important for hair growth and regeneration, and could be a potential treatment for hair loss.

Hair casts, also called pseudonits, are often mistaken for other conditions.

Untreated Sheehan's Syndrome caused severe heart failure in a woman, which improved with hormone and heart failure treatment.

HBM-based nursing intervention improved medication compliance, reduced negative emotions, and enhanced quality of life for renal transplant recipients.

Netherton Syndrome can cause severe skin lesions in rare cases.

Female nursing students with iron deficiency anemia have poor knowledge and practices regarding iron intake, needing better health education and physical monitoring.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

Netherton's syndrome can cause frequent bacterial infections beyond just skin issues.