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A young woman with late-stage Vogt-Koyanagi-Harada disease was successfully treated at a hospital.

Carpronium chloride increases blood flow by widening small blood vessels.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

ATP-sensitive potassium channels play a role in chloroquine-induced itch in mice.

Rat hair follicle stem cells can be used to improve blood vessel growth in engineered skin.

Differences in androgen receptor expression and tissue properties may lead to higher cryptorchidism risk in certain rats.

LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

Certain gene combinations improve cashmere quality and production in Liaoning goats.

A person with a new mutation in the SCN1A gene developed brain inflammation after COVID-19.

A genetic variant in the KRT25 gene causes tightly curled hair.

Involucrin is a useful marker for keratinocyte differentiation in mice.

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ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

People with androgenetic alopecia have a higher risk of heart disease.

Overexpression of activin A in mice skin causes skin thickening, fibrosis, and improved wound healing.

AC-5216 reduces anxiety in mice through neurosteroids affecting GABAA receptors.

Blocking certain receptors in the lungs might help treat a specific type of asthma.

A JAK1 variant causes hair loss, skin issues, and thyroid disease, but treatment with a specific inhibitor can help.

Early genetic testing and zinc therapy are crucial for managing acrodermatitis enteropathica effectively.

A 4-year-old boy with a rare type of rickets and hair loss improved in bone health but not hair growth after vitamin D and calcium treatment.

Normal cells outcompete and remove mutant cells in the pancreas with the help of the EphA2 receptor.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.

Upadacitinib helped regrow hair and maintain ulcerative colitis remission.

Ciproterone acetate improves hair regrowth and acne in most female patients.