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Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

KLHL24-mutant stem cells help understand skin and heart disease.

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The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.

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The fragrance cyclohexyl salicylate helps promote hair growth and increase hair stem cell numbers.

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The patient responded well to treatment with no disease progression.

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The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

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Mutations in the LSS gene cause a rare type of hereditary hair loss.