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Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

Hairless mammals evolved quickly in both gene and non-gene areas related to skin and hair.

Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Certain genetic differences may affect how likely someone is to get COVID-19 and how severe it might be.

Blocking the JAK/STAT pathway may help reduce skin sensitivity in Xeroderma pigmentosum.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

A cancer patient's hair became permanently curly after treatment with nivolumab.