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Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

A patient with untreated congenital adrenal hyperplasia had large benign tumors in her adrenal glands removed, improving her symptoms.

Cardiomyocyte-derived media can inhibit lung cancer cell growth and movement.

Cortexolone 17a-propionate may be an effective new treatment for hair loss.

Children and adults with Cushing's disease show different symptoms and males have more severe cases; surgery outcomes can be predicted by certain factors.

A new method accurately measures molecular movement without complex modeling.

MPZL3 protein helps keep sebaceous gland size and cell growth in check.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

A woman with EMS showed unusual skin mucinosis without the typical hard skin syndrome, suggesting EMS can cause skin mucinosis.