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Lowering homocyst(e)ine levels can reverse skin and hair lightening by restoring enzyme activity needed for pigmentation.

Two new gene mutations cause a rare hair disorder.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

Some patients with severe alopecia areata developed skin darkening from their treatment, which may indicate a less effective response to the therapy.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

A 91-year-old woman's hair turned black in one spot, with skin changes underneath.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Stem cells in the eye have different roles and behaviors, helping maintain and repair the eye's surface.

SASH1 gene mutations are linked to various inherited skin pigmentation disorders.