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

Dissecting cellulitis of the scalp is a condition that causes inflammation and scarring on the scalp, mainly affecting African-American men, and can lead to permanent hair loss.

Dexamethasone reduces inflammation and delays skin cell changes caused by TPA.

Disrupting a specific protein's function in hair follicle stem cells triggers their activation and a self-healing process.

Researchers found a new sign of fungal infection in some patients with Seborrheic Dermatitis.

Lower SMAD2/3 activation predicts more severe skin cancer.

Researchers found specific genes in the part of hair follicles that could help treat hair disorders.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

The methods tested are reliable for assessing dandruff reduction.

New methods efficiently isolate dermal papilla cells from hair follicles, preserving their characteristics better than traditional methods.

Discoid lupus erythematosus involves immune activation and fibrosis around hair follicles, with shared pathways across humans, dogs, and mice, suggesting potential treatments for both humans and animals.

The VSCAPSI is a helpful method for evaluating the severity of scalp psoriasis.

Discoid Lupus Erythematosus causes scalp plaques that can lead to hair loss, and antimalarial drugs are effective treatments.

Proper niche formation in Drosophila requires Slit-Robo signaling for cell migration.

Dermoscopy has greatly improved the diagnosis of skin lesions and our understanding of their morphology and biology.

CSC is linked to mineralocorticoid receptor damage, stress, and steroid use, with treatments including drugs and laser therapies to prevent eye damage.

3D spheroid culture makes stem cells better at reducing inflammation.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

S-1 treatment led to a complete response in pancreatic cancer with manageable side effects.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Scube3 gene affects mouse embryo growth in multiple areas, but needs more research.

VDUP1 is found in skin and hair follicles, interacts with sciellin, and may help regulate skin cell differentiation.

Genetic testing can diagnose hair loss linked to DSG4 gene variants.

The search scheme SMRI is faster and more secure for retrieving encrypted data from the cloud.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

Diphencyprone (DCP) is an effective treatment for severe alopecia areata and resistant warts, with some risks.

Human dermal stem cells can become functional skin pigment cells.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

ADSC injections improve hair density, thickness, and reduce inflammation in female pattern hair loss.