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Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Terbinafine effectively stops fungal invasion of human keratin.

SARS-CoV-2 proteins help the virus avoid the immune system, delaying response and increasing inflammation.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

NBCCS and BFHS might be the same syndrome, helping better identify and manage cases.

The G allele of IFITM3 rs12252 is linked to more severe COVID-19.

A cat had a rare fungal infection caused by Microsporum gypseum.

The grey patch variant of tinea capitis is most common, mainly spread through family and animals.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

A calf in Scotland likely had Schmallenberg virus from its mother.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

PC-associated alopecia has unique microscopic features.

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

GLPLS and LPP are variants of lichen planus.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

The newborn's skin blistering is due to a genetic condition called epidermolytic hyperkeratosis.

A young man developed a rare, bilateral scalp condition after head trauma, causing hair loss but no neurological or eye issues.

Monilethrix hair issues are due to problems in the hair's internodes.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

Rizatriptan benzoate-loaded dissolving microneedles are effective and convenient for treating acute migraines.

VCAM1 appears early in kidney injury and signals future nephron loss.

Different skin diseases show unique patterns of skin cell separation, cell death, and granular layer changes.

Clq deficiency is linked to systemic lupus erythematosus symptoms.

Some cases of folliculotropic mycosis fungoides may progress slowly and not need aggressive treatment.

Ossification in trichilemmal cysts is more common than previously believed.