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New compounds show promise for treating hair loss, enlarged prostate, and prostate cancer, with some being more effective and having different side effects than current treatments.

Green tea component EGCG may help prevent hair loss by changing microRNA levels in certain scalp cells.

A cancer drug called nilotinib might cause hair loss due to inflammation around hair follicles.

Women with greater androgen sensitivity respond better to finasteride for hair loss.

The X5 Hairlaser might help treat male hair loss, but more research is needed.

Genomic approach finds new possible treatments for hair loss.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Mutation in hairless gene may increase hair loss risk.

Men with a certain type of hair loss often use facial moisturizers, and a specific antibiotic treatment may help another hair condition.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

JAGGED1 could help regenerate tissues for bone loss and heart damage if delivered correctly.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

There are many treatments for common hair loss, but more trials are needed to decide which are best.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

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

The protein StAR is found in 17 different organs and can affect hair loss and brain functions, but its full role is not yet fully understood.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Researchers found a gene mutation responsible for a rare hair loss condition.

Troxerutin helps protect skin cells from oxidative stress and may be good for treating hair loss.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

Androgenic Alopecia, a common hair loss condition, can be effectively treated with finasteride and other treatments.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

High aldosterone and free testosterone levels link to female hair loss; testing aldosterone may predict hypertension risk.

Obesity worsens Polycystic Ovary Syndrome symptoms, and weight loss is a key treatment.

Researchers created immortal human skin cells with constant testosterone receptor activity to study hair loss and test treatments.

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

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

Androgens like testosterone affect skin health and can lead to conditions such as acne and hair loss, with various treatments available.

S100A4 and S100A6 proteins may activate stem cells for hair follicle regeneration and could be potential targets for hair loss treatments.