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Heat-treated Limosilactobacillus fermentum with menthol, salicylic acid, and panthenol promotes hair growth and balances scalp microbiome in people with androgenetic alopecia.

Gene linked to common hair loss found, may lead to new treatments.

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

PDGF-BB helps young melanocytes grow but stops mature ones from growing, and it makes melanocytes more specialized.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

SLC45A2 and GPNMB genes help control chicken feather color by promoting melanin.

Pleuropterus multiflorus shows promise as a safe and effective treatment for androgenetic alopecia.

Further testing of paclitaxel poliglumex for this cancer treatment is not justified.

Laminin-511 may help promote hair growth, while laminin-332 does not affect hair loss.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

A new DSG4 gene mutation causes hair defects in a young girl.

A new treatment for hair loss shows promise with fewer side effects.

ALDOA levels drop in hair cells during hair loss.

CTP-543 significantly improved eyebrow and eyelash regrowth and patient satisfaction in adults with alopecia areata.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

PCE-DP brightens skin and promotes hair growth by enhancing cell growth and reducing melanin uptake.

Grape seed extract may safely and effectively help prevent lung cancer.

A new treatment using unactivated platelet leukocyte autoplasma cured 80% of non-scarring alopecia patients.

NonClassic Congenital Adrenal Hyperplasia is a less severe form of a genetic disorder affecting adrenal gland function.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps from birth.

Combining low-level laser therapy with scalp microneedling and a clobetasol solution significantly improves androgenetic alopecia.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

HGF combined with ADA is highly accurate for diagnosing tuberculous pleural effusion, especially in younger females.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.