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Diphenylcyclopropenone is effective and safe for treating severe alopecia areata in children, with maintenance therapy reducing relapse risk.

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

DEC cells show promise as a safe and effective treatment for Duchenne muscular dystrophy.

EPDS and MS might share an immune-related cause.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

PICAT is a reliable tool for assessing dermatology residents' skills in PRP procedures for hair loss.

Electric pulses can effectively activate platelets and release growth factors, offering a better alternative to traditional methods.

Biopsy is crucial to accurately distinguish Erosive Pustular Dermatosis of the Scalp from Squamous Cell Carcinoma.

PDRN helps repair tissue and improve wound healing with a high safety profile.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Diphenylcyclopropenone (DPCP) is more effective than anthralin for treating resistant alopecia areata.

FDA-cleared devices often fail to produce high-quality platelet-rich plasma consistently.

High leptin levels may promote skin cancer and inflammation, suggesting potential for leptin-targeted therapies.

Diphenylcyclopropenone (DPCP) effectively treated both alopecia areata and verruca vulgaris.

The cerium-polypeptide hydrogel effectively heals drug-resistant bacterial wounds by fighting bacteria, reducing inflammation, and promoting tissue repair.

A new pain-measuring system using sensors and AI can effectively detect pain in mice, which may help assess pain in humans and develop treatments.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

DAB labeling effectively identifies collagen type III and PDGFR in horse skin, but may show false positives.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

A rare scalp condition called Erosive pustular dermatosis is hard to diagnose and treat.

ATP-sensitive potassium channels are important for hair growth.

A new method improves the isolation of hair follicle cells for better hair growth research.

Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

Popliteal Artery Entrapment Syndrome (PAES) is a rare but possible cause of leg pain during walking, even in untrained women.

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

Chronic scalp lesions with crusts and pus that heal with strong topical steroids suggest Erosive Pustular Dermatosis, confirmed by biopsy showing specific immune cells.

A patient with total hair loss developed vitiligo after using a treatment called DCP.