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Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

A specific gene mutation causes woolly hair and hair loss.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

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A man had two rare autoimmune diseases that might be connected.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

OR101 may effectively treat atopic dermatitis and similar skin conditions.

The SHJH hr mice with a mutated Hr gene show signs of faster skin aging due to poor antioxidative protection.

UC.145 may be a new biomarker for predicting gastric cancer.

New compounds show promise as nonsteroidal treatments for hair loss.

Four new FGF5 gene variants cause long hair in dogs.

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A gene mutation in mice causes severe skin disorder similar to a human condition.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

20(S)-Protopanaxadiol-aglycone may help prevent and treat prostate cancer by reducing androgen receptor activity.

A new method allows for controlled, long-lasting delivery of retinoic acid through the skin with less inflammation.