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A woman's liver was damaged by taking the herbal supplement Shou-Wu-Pian, but it got better after she stopped using it.

There's no link between hair loss type androgenic alopecia and benign prostatic hyperplasia, but early hair loss and family history can mean more severe alopecia.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

Herpes simplex virus infections should be considered in pemphigus patients to avoid unnecessary changes in treatment.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

Most men with lichen planopilaris had it confirmed by biopsy and often had thyroid issues, sexual dysfunction, or prostate cancer, hinting at a link with hormonal problems.

The document explains that hirsutism, often caused by hormonal issues, can be managed with treatment to improve both physical appearance and mental health.

Valproic acid helps hair follicle stem cells survive better in low oxygen and glucose conditions.

Visual field defects in lupus nephritis can be caused by hypertensive retinopathy, not glaucoma or medication toxicity.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

PTHrP regulates various normal body functions, including bone development, skin, and muscle function.

PRP treatment can safely improve short-term vision in acute NAION patients.

A rare combination of halo nevi, nonsegmental vitiligo, and early gray hair can occur together.

Losartan may help treat Postural Orthostatic Tachycardia Syndrome (POTS) symptoms.

A rare autoimmune disease caused the woman's scalp blisters and hair loss, successfully treated with medication.

A new compound, HTPI, promotes hair growth by protecting cells from damage and regulating energy use.

p2y5, now called LPA6, is a receptor important for human hair growth.

DPCP alone is more effective and safer for treating chronic extensive alopecia areata than combining it with anthralin.

Early diagnosis and multidisciplinary care are crucial for managing PCOS in adolescents.

Lichen planopilaris is a chronic, scarring hair loss condition with no definitive cure, requiring accurate diagnosis and treatment to manage symptoms.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

Women with hair loss should be checked for PCOS, as it's often related and early diagnosis can help with treatment.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

Finasteride can cause serious side effects in some men, needing more research for treatment.

The solution increased hair density safely and effectively for hair loss.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

The 2018 ISPAN Meeting emphasized hands-on learning, patient safety, and professional growth in medical aesthetics and reconstructive practices.