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The Exfoliate-Dissolve-Repair skincare approach may effectively treat keratosis pilaris and reduce the need for corticosteroids.

Lifestyle changes can help manage androgenetic alopecia.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

Upadacitinib improved symptoms and hair regrowth in a teen with multiple autoimmune conditions.

Extracellular vesicles can worsen Alzheimer's but also offer potential for diagnosis and treatment.

Special cells can help regrow hair in alopecia areata.

Björnstad syndrome can cause hair loss similar to androgenetic alopecia, and treatment with baricitinib and minoxidil may help.

Smart biomaterials and dressings show promise in treating chronic skin diseases by improving drug delivery and minimizing side effects.

Imbalanced skin microbiome can worsen skin conditions like acne and eczema.

Improving blood vessel health and controlling uric acid may help manage alopecia areata.

Certain fungi may contribute to hair loss in cynomolgus macaques.

BMS-470539 reduces skin fibrosis and inflammation.

Demodex mites may contribute to acne and rosacea by disrupting skin balance.

HLD10 can include increased body hair and Mongolian spots.

Half-siblings with a rare skin condition improved with treatment for a fungal infection, but hair loss remained.

UVA exposure worsens hair loss by activating a specific cell pathway.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

CD4 T cells need IFN-γ to cause hair loss in alopecia areata.

Blue light therapy is promising for skin and hair conditions but needs more research for widespread use.

Restoring skin microbial balance may help treat acne.

Microsporum spp. is the most common fungus causing skin infections in dogs.

Reducing neutrophils or inhibiting NETs improves wound healing in sickle cell disease.

Patients with thyroid disorders show different symptoms and antibody levels.

An extremely low-birthweight infant had a rare genetic skin disease and died despite treatment.

Ayme-Gripp Syndrome was confirmed in a woman through genetic testing, highlighting the need to consider rare genetic conditions in diagnoses.

The Fas/FasL pathway may play a role in alopecia areata.

Diet changes can improve skin health by altering the immune response and skin microbiome.

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

Recent selection on immune response genes was identified across seven ethnicities.