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Finasteride, when given in high oral doses to pregnant monkeys, caused genital abnormalities in male fetuses, but not in female fetuses or those exposed to intravenous finasteride.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Hair follicle stem cells can become corneal-like cells with the right environment.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Inositol helped cure hair loss around rats' eyes and improved their growth.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

Stem and progenitor cells in the eye have different division rates and locations, affecting how they respond to injury.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

A new DSG4 gene mutation causes hair defects in a young girl.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.

miR-3606-3p reduces skin fibrosis by blocking key signaling pathways.

Hair restoration surgery can change the appearance of hair when examined with a special magnifying tool.

Most skin conditions in Down syndrome are benign and involve dry or thickened skin.

A new mutation in the ST14 gene was found in a patient with ARIH syndrome, showing milder symptoms and no tooth issues.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

The newborn's skin condition improved over time, leaving only lighter skin patches.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Sebaceous lipids are crucial for keeping skin and eyes healthy in mice.

New treatments using stem cells and special materials show promise for severe eye surface disease.

The cornea develops independently of the lens, following its own default pathway.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

The orphaned foal stayed healthy despite challenges, showing the need for thorough health checks.

Early recognition of symptoms is crucial for treating IPEX syndrome with a stem cell transplant.

A 12-year-old boy with twenty nail dystrophy, a condition affecting all nails, was treated conservatively due to its self-limiting nature and good prognosis.

Combining microneedling with either vitamin D3 or bimatoprost improves hair regrowth more than microneedling alone.

Latanoprost eye drops may cause skin depigmentation.

MicroRNA-22-3p hinders hair regrowth in male pattern baldness by affecting a specific protein.