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Ectoin helps prevent cortisone-induced skin problems and supports skin health.

Two plywood factory workers developed contact dermatitis from phenol-formaldehyde resin, a known allergen.

A man had a rare skin reaction from a hair loss medication, which improved after stopping the drug.

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

Annexin A2 isoform 2 helps dermal papillae cells grow, affecting hair growth.

Astrotactin-2 is cleaved in a specific way that helps understand its maturation.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

Skin reactions to drugs are common and can be deadly, usually requiring stopping the drug and may be better prevented with genetic testing in the future.

EGFR deficiency in skin causes hair follicle issues and inflammation.

EETs can delay seizures by affecting GABA activity, offering potential new treatments for seizures.

ILC1-like cells can cause alopecia areata by themselves.

People with anhidrotic ectodermal dysplasia may get severe bronchitis if exposed to dust.

A rare skin reaction from cancer treatment was successfully managed with topical treatments and antihistamines.

GABEB is a less severe skin condition caused by a gene mutation affecting collagen, leading to blisters and other symptoms.

Lack of cystatin M/E causes thin hair and dry skin.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

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

Epitestosterone may counteract testosterone's effects and has roles in body processes like prostate growth and hair distribution.

Poly(ADP-ribose) synthesis is linked to skin cell differentiation.

Staphylococcus epidermidis A/C strains are more antibiotic-resistant and infection-adapted, while B strains thrive in hair follicles.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

A unique gene mutation was found in a family with monilethrix.

PRIDE complex side effects from EGFR inhibitors can be managed without stopping treatment.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Researchers found two new genetic variants linked to Alzheimer's disease.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

Mutations in specific genes disrupt development of sweat glands, teeth, hair, skin, and nails in HED.