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In this study, researchers identified a novel homozygous variant in the FAM83G gene responsible for autosomal recessively inherited palmoplantar keratoderma with curly hair in a consanguineous Pakistani family, suggesting FAM83G plays a crucial role in skin and hair homeostasis.

This article discusses various dermatological studies cited by previous authors and reports no new clinical results.

New mutations in the hairless gene may cause hair loss and affect bone development.

A mutation in the KRT25 gene causes a rare hair disorder with thin, woolly hair.

This study identified two prevalent and one newly proposed founder LIPH mutations in Japanese patients with autosomal recessive woolly hair/hypotrichosis and associated these mutations with different severities of hair loss.