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PEVIII is a promising treatment for Pseudomonas aeruginosa keratitis.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Pseudopelade of Brocq is hard to diagnose and treat, with limited effective options.

3D models from confocal microscopy improve melanoma detection on sun-damaged skin.

Vitamin B12 deficiency can cause reversible skin darkening.

A Rathke's cleft cyst caused hormonal imbalances and symptoms in a 68-year-old woman.

Acitretin can cause excess tissue growth and hair loss.

Solid Lipid Particle technology makes retinol more stable, effective, and gentle on the skin.

A woman was diagnosed with porphyria cutanea tarda and improved with phlebotomy and lifestyle changes.

A specific microRNA, chi-miR-30b-5p, slows down the growth of hair-related cells by affecting the CaMKIIδ gene in cashmere goats.

If someone has scaly skin, muscle stiffness, and intellectual disability, doctors should consider Sjogren-Larsson Syndrome, but other conditions if more symptoms are present.

Certain medications and smaller pupil size increase the risk of intraoperative floppy iris syndrome during eye surgery.

Sonidegib often causes hair loss, and LC-OCT helps identify early signs.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

Using topical prostaglandin F2α for glaucoma may cause loss of eyelash or eyebrow pigment.

The project highlights the importance of early diagnosis and patient advocacy in managing Systemic Lupus Erythematosus.

Trichoscopic evaluation is important for assessing hair loss in women.

Retinoids help manage skin conditions in black individuals.

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

A new method allows for controlled, long-lasting delivery of retinoic acid through the skin with less inflammation.

Researchers found a new mutation causing total hair loss from birth.

Rathke’s cleft cysts can rarely cause Cushing disease, and surgery can improve symptoms.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

RORA plays a key role in controlling seasonal hair molting by affecting hair follicle cell activity.

A woman kept her eyelashes during chemotherapy possibly because of her glaucoma eye drops.

CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

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

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.