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Combined microneedling with minoxidil improves hair growth more than minoxidil alone but may cause mild side effects.

Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.

A substance from Caulerpa racemosa seaweed may protect against skin damage caused by air pollution by reducing oxidative stress and cell death.

Cladribine has known risks and potential new safety concerns, requiring careful monitoring.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

A woman with both Cronkhite-Canada syndrome and myelodysplastic syndrome improved significantly with corticosteroid treatment.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.

The workshop discussed the role of a protein called calreticulin in health and disease, its potential as a treatment target, and its possible use as a disease marker.

MCTD should be considered in children with recurring muscle issues, lupus-like symptoms, and edema.

WomenCare helps predict PCOD risk in women to encourage early medical consultation.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

Individualized treatments may help manage Dercum's disease symptoms.

A 5-year-old girl with a rare skin disorder was effectively treated with skin creams instead of oral medication.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

A woman with HIV had a severe skin condition that improved with antiretroviral therapy.

CRISPR gene editing reduces harmful molecules in cells from Emery–Dreifuss Muscular Dystrophy patients.

CRH in the skin acts like the body's stress response system, affecting cell behavior and immune activity.

CDK inhibitors may help treat ARDS and psoriasis but need more testing for safety and effectiveness.

DPR can cause skin, hair, and nail issues, sometimes appearing later in life.

Cyclic ADP-ribose helps regulate calcium and signals that promote hair growth in hair follicle cells.

High CRP levels could indicate vitamin D deficiency in people with alopecia areata.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

PRIDE syndrome helps identify skin side effects from EGFR inhibitors like erlotinib.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Clinicians should consider individual factors and communicate risks and benefits when prescribing ritlecitinib for adolescent alopecia areata.

CCCA may involve the PD1/PDL1 pathway and increased caspase 3, leading to permanent hair loss.

Neural crest-derived progenitor cells in the cornea could help treat corneal issues without transplants.

Small bowel lesions in Cronkhite-Canada syndrome persist despite steroid treatment.

A CCS patient with severe complications was successfully treated using combined therapies.