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Parry–Romberg Syndrome can involve the brain even without obvious symptoms, and a new diagnostic framework is suggested for early detection.

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The regulations aimed to improve domiciliary care in Wales by ensuring better work conditions and visit schedules.

Recognizing new allergens can help reduce contact dermatitis cases.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

CLASI is a valid tool for assessing skin activity and damage in lupus patients.

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Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

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Solidified SEDDS improve drug stability and bioavailability better than liquid SEDDS.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Using both DLQI and Skindex-16 together gives a better understanding of quality of life in skin disease patients.

Risankizumab effectively treats and maintains skin clearance in moderate-to-severe psoriasis.

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GI197111X is best dissolved in Capmul MCM for trials.

Interface dermatitis is the most common skin change in drug-induced hypersensitivity syndrome.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

The authors suggest using a standard system to name hair grafts to improve communication in hair restoration.

Seven genetic variations in sheep's DSG4 gene are linked and affect wool traits.

Researchers identified genes linked to coat color, body size, cashmere production, and high altitude adaptation in goats.