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Testosterone with finasteride improved muscle and bone health in men with spinal cord injury.

Narrowband UVB phototherapy alone is not very effective for treating alopecia areata.

A woman's hair loss and skin discoloration were found to be caused by a rare case of leprosy on the scalp, not alopecia-vitiligo overlap.

Triamcinolone acetonide therapy for hair loss may cause a skin condition called linear lichen planus.

Vismodegib effectively treats advanced basal cell carcinoma but requires careful management of serious side effects.

Photobiomodulation therapy may help treat hair loss in people with darker skin, but more research is needed.

Early diagnosis of PSIS can lead to normal height with growth hormone and testosterone treatment.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

A gene mutation in mice causes severe skin disorder similar to a human condition.

A 4-year-old girl with a rare lupus condition was successfully treated with oral corticosteroids, leading to full recovery and hair regrowth.

Bariatric surgery improves ovulation rates in women with PCOS and obesity better than medical therapy.

The newborn was diagnosed with a rare skin disorder causing blisters, which requires careful wound care and family support.

Bcl-2 affects hair growth and pigmentation by controlling cell death.

Low-level laser therapy, now called photobiomodulation, is recognized for its broad medical applications and scientific backing.

A rare form of lupus caused hair loss and skin bumps, diagnosed through biopsy, improved partially with treatment.

Hair loss was likely caused by gymnastics activities on a balance beam.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Treating generalized granuloma annulare is difficult, with PUVA being the most effective option, but relapses are common.

CNGA3, GLUD1, and SIRT1 are promising targets for treating aging and glioblastoma.

Reduced alpha smooth muscle actin may cause hair loss in androgenetic alopecia.

A vaccine may prevent benign prostatic hyperplasia (BPH).

Mesotherapy with bicalutamide has limited effectiveness for female hair loss.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Congenital atrichia with papular lesions causes permanent hair loss in children.

Biotin improved hair appearance in uncombable hair syndrome but didn't change hair structure.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

VPS13C variants are linked to more severe REM sleep disorder and faster progression to Parkinson's disease.