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A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

A new syndrome may link skin, growth, mental, and hair issues.

Ruxolitinib helped a patient with alopecia areata regrow hair.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

A 10-year-old boy's nail condition is mainly cosmetic and improves over time with treatment.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Progeria causes early aging due to a gene mutation, affecting skin, bones, and heart, with treatments aimed at improving life quality.

Goats can have various genetic skin diseases affecting hair, skin, and thyroid function.

Patients with cutaneous lupus erythematosus have a higher risk of skin cancer and other cancers.