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HS patients rarely see dermatologists, often get opiates, and need better care.

Two new gene clusters important for hair formation were found on human chromosome 11.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Two new gene clusters important for hair formation were found on human chromosome 11.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

TH antibodies in vitiligo and AA patients recognize the same protein parts.

16-MHA can restore damaged hair's protective barrier and moisture balance.

The hydrogel dressing effectively treats infected wounds by combining infection control and tissue regeneration.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

HDAC inhibitors help brain cells grow and improve brain function.

The AI model accurately classifies Alopecia Areata with 96.94% accuracy.

Metabolite 7 is a strong inhibitor for Alzheimer's disease management.

Higher PHGDH levels cause unusual melanin buildup in hair follicles.

B6.Cg-Tyr c−2J Hr hr /J mice have a stronger delayed sunburn reaction and are good for UV research.

Higher FABP4 levels may indicate more severe alopecia areata.

HASHA is a safe and effective option for chin augmentation.

Newly designed proteins can effectively degrade specific proteins in cells, offering a promising alternative for targeted protein degradation.

VDDR I and II are genetic disorders affecting vitamin D use, causing rickets, with VDDR I treatable by vitamin D supplements and VDDR II needing high doses and calcium.

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ARQ-234, a protein designed to treat atopic dermatitis, shows increased effectiveness in early testing.

ATP6AP1‐CDG can cause hearing loss, hair loss, and protein issues, even in female carriers.

Biotin supplements significantly improved a young girl's uncombable hair.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Adalimumab may cause severe hair loss in some patients.

AB+ blood group is more common in alopecia areata patients.

AnnoPharma effectively identifies substances causing adverse drug reactions in medical abstracts.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

Scientists found a gene in mice that causes early hearing loss.