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The report found a new type of hair loss in African-American women that affects more areas of the scalp than previously thought.

Applying pseudoceramide improved skin and hair health.

Anti-Desmocollin 3 antibodies can cause atypical pemphigus symptoms.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

The interdisciplinary approach improved the quality of life for a Parkinson's patient and eased staff workload.

Immune privilege collapse in hair follicles may cause permanent hair loss in certain conditions.

A 21-year-old male with a rare genetic disorder experienced sudden hair loss and high DHEAS levels, likely due to a condition similar to PCOS, usually seen in women.

An elderly man's non-healing scalp lesion was successfully treated with a strong topical steroid.

The treatment for alopecia areata with diphenylcyclopropenone was unsuccessful.

An 84-year-old man got a rare scalp condition from using imiquimod cream, which was cured with systemic steroids.

Penicillium might rarely cause scalp infection in children.

Finasteride may cause floppy-iris syndrome during cataract surgery, so check patients' medical history.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

iEdgePathDDA effectively finds new drug-disease links, outperforming other methods.

PRP injections are safe but don't significantly improve Peyronie's Disease.

KID syndrome should be reclassified as an ectodermal dysplasia.

The updated criteria improve the accuracy of diagnosing lupus.

A woman had a rare infection of both white piedra and head lice, which improved after 10 weeks of antifungal treatment.

Phosphodiesterase inhibitors like tadalafil can reduce cell growth in BPH caused by CD8+ T cells in low androgen conditions.

High-dose intravenous iron therapy doesn't interfere with treatment improvements in IBD patients with iron deficiency anemia.

The woman has a rare skin condition called follicular Dowling-Degos disease, which has limited treatment options.

Pityriasis rubra pilaris is a rare skin disorder with reddish-orange patches and thickened skin, needing better treatment understanding.

ATP-sensitive potassium channels are important for hair growth.

Pembrolizumab can cause serious liver issues, requiring close monitoring and early treatment.

CCCA affects Black men too, with a genetic link found in the PADI3 gene.

Prednisolone improved symptoms in a woman with Cronkhite-Canada syndrome, but regular screenings are needed due to cancer risk.

CTIP2 may help in skin development and maintenance.

Erosive pustular dermatosis of the scalp is a type of skin inflammation often confused with other conditions, requiring continuous treatment.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.