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Rezpegaldesleukin shows promise for treating severe alopecia areata.

The new wound dressing helps skin heal faster and fights infection.

Weak cell junctions disrupt hair follicle stem cell rest.

The microneedle arrays effectively promote wound healing and have potential for clinical use.

Zinc oxide nanoparticles in sunscreen do not penetrate deep into the skin.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Oral zinc gluconate and topical steroids significantly improved a rare scalp condition in three elderly patients.

Early diagnosis of trachyonychia improves treatment and reduces psychological and cosmetic issues.

Chinese patients with alopecia areata value JAK inhibitors but worry about side effects and relapse, highlighting the need for education and support.

Carbamazepine caused hair loss in a man, which stopped after he stopped taking the drug.

A 10-year-old boy with abnormal genital development had surgery and tests to find the cause and plan treatment.

The conclusion suggests that the zinc lozenge study is valid despite imperfect blinding, as many participants could not correctly identify their lozenge type.

BST2 is a key marker for hair loss disease alopecia areata.

Minoxidil treatment improves heart defects in a DiGeorge syndrome model.

Isoallopregnanolone may be a safe and effective treatment for reducing tics in a mouse model of Tourette syndrome.

SEFFI is a safe and effective anti-aging treatment with few complications.

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

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

Growth hormone therapy can improve growth in Netherton syndrome patients with growth hormone deficiency.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

People with certain hair disorders may also have missing permanent teeth.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Oral zinc sulphate effectively treats alopecia areata with few side effects.