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PEVIII is a promising treatment for Pseudomonas aeruginosa keratitis.

Surgical removal is advised for large congenital blue nevi due to rare cancer risk.

Surgical removal of abnormal fat pads fixed the woman's eyelid issue caused by likely silicone injections.

The conclusion is that Darier-White disease was accurately described by White but he missed the key feature of dyskeratotic cells which Darier identified.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Mutations in certain skin proteins cause severe skin issues, while others have limited effects, highlighting the need to understand these proteins for better treatments.

Cantú syndrome may be linked to pituitary adenomas.

Melanocyte pathology requires keratinocyte hyperplasia and regulation dysfunction.

A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.

MOF controls skin development by regulating genes for mitochondria and cilia.

Long-term use of difluprednate eye drops in dogs can lead to hair loss and hormone imbalance.

A cat developed a skin lesion from a topical solution, which healed with minoxidil treatment.

EGFR deficiency in skin causes hair follicle issues and inflammation.

A rare skin condition causes red and dark patches on the face and limbs.

Specific mutations in a receptor cause facial abnormalities and hair loss.

Researchers created a new mouse model for studying scleroderma.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Dermoscopy is useful for identifying skin lesions in dogs, with specific features distinguishing infundibular keratinising acanthomas from follicular cysts.

Avoiding damage and using specific shampoo and supplements improved the hair condition.

Coriaria sinica Maxim extract speeds up burn healing and hair growth in rats.

Meis2 is essential for whisker development, independent of nerve involvement.

A woman got a scalp condition from using latanoprost, but it improved after stopping the drug and starting other treatments.

A 90-year-old woman's hand lesion was a rare, aggressive skin cancer treated successfully with surgery.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Parry Romberg syndrome requires awareness and teamwork in primary care for proper diagnosis and management.

A rare gene variant causes hair and nail issues in a family.

Chronic cutaneous lupus erythematosus causes scarring, hair loss, and skin discoloration, especially on sun-exposed areas.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

Anti-CD19 therapy may help treat SLE and NMOSD.