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Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

A rare scalp condition, cutis verticis gyrata, was found in a woman with primary scarring alopecia.

Platelet-rich plasma treatment shows early improvement in femoral head avascular necrosis.

Women with congenital adrenal hyperplasia showed no prostatic growth.

Hair-shaft abnormalities can indicate neurological disorders, some of which are treatable.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

A young girl had a rare neck cyst removed and needs careful monitoring for related health issues.

Airway issues can occur in Conradi–Hünermann–Happle syndrome and can be managed with minimally invasive procedures.