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The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requires high doses of calcium and vitamin D for management.

A gene mutation causes curly hair and hair loss in rats.

A woman had a delayed allergic reaction to the blood thinner enoxaparin, treated with a steroid cream.

Higher CSF 5-HIAA levels may predict better response to serotonin re-uptake inhibitors in trichotillomania.

RHUPUS should be considered in children with deforming arthritis.

Estrone and 17β-estradiol levels in hair differ between males and females.

REVIVV® serum improves hair growth and reduces shedding in androgenetic alopecia.

Hair follicle stem cells can become heart muscle cells.

Ultraviolet techniques help identify Grover’s Disease, which may be underdiagnosed in young people and females.

RORA affects hair follicle stem cells' structure and movement, potentially helping treat hair loss.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

Isoproterenol helps hair follicle stem cells turn into beating heart muscle cells.

COVID-19 vaccination is generally safe for people with Hidradenitis Suppurativa.

Human hair follicle stem cells can become endothelial cells with certain growth factors, useful for vascular treatments.

Chronic graft-versus-host disease in the skin shows strong Th1 immune response and unique barrier issues.

A defective protein in progeria causes cell death and atherosclerosis, but a treatment targeting cell stress may reduce these effects.

Herpes zoster infection can cause permanent hair color change in the affected area.

UVB radiation harms hair growth and health, causing cell death and other changes in human hair follicles.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

Osthole inhibits the TRPV3 channel by binding to specific sites, potentially aiding drug development for skin diseases and cancers.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Treating PCOS patients with HP HMG significantly raises the risk of ovarian hyperstimulation syndrome, needing careful dose management.

Cannabidivarin (CBDV) helps new brain cells grow and develop in a specific brain area through a certain receptor.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

Vitamin D receptor is crucial for skin wound healing.

K31 can identify clear secretory cells in human sweat glands.