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A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The combination of the excimer lamp and liquor carbonis detergens is more effective for scalp psoriasis than the lamp alone.

The genetic variation in the KAP13-3 gene may affect cashmere fiber traits in Liaoning goats.

Leporacarus gibbus mite was found in a domestic rabbit in Espírito Santo, Brazil, for the first time.

A rare lupus case in Bangladesh improved with specific treatment.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

Papillon-Lefèvre Syndrome causes early tooth loss and skin issues, needing early dental diagnosis.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

Neutrophils quickly respond to skin injury.

The PCL/PHB blend allows for slower, more controlled curcumin release than individual polymers.

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A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

Using laccase to add poly(tyrosine) to wool makes it less likely to shrink and stronger.

SIG-1451 could be a promising new treatment for atopic dermatitis.

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The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

Lygodium japonicum spores can reduce inflammation by blocking certain cell signals.

Leflunomide successfully treated a rare skin condition in a liver transplant patient.