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Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

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

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Thevetia peruviana bark extract reduces pain in mice and may help create new painkillers.

Monilethrix causes brittle hair and hair loss, and it runs in families.

Linoleic acid is important for healthy skin, and while most people get enough from their diet, not having enough can cause skin and hair problems.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Alpinia calcarata, Alpinia galanga, and Alpinia zerumbet have potential health benefits, including fiber, antimicrobial, antioxidant, and cardiovascular properties.

Lupus patients in Ghana face healthcare challenges, and the Oyemam Autoimmune Foundation is working to improve awareness and support.

Many in Saudi Arabia experience early hair loss but lack awareness of treatments.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Linoleic acid is essential for healthy skin, and while deficiency is rare in Western societies, it can cause dry, scaly skin and hair loss.

Polycystic ovaries and early male baldness are inherited traits.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Key genes and pathways influence wool traits in Merino sheep.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Eating vegetarian, having allergies, and family history might be linked to getting gray hair early.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Scientists found 53 keratin genes in yaks that are important for hair growth and share similarities with those in other animals.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Local healers in Addis Ababa use 81 medicinal plants, mainly from the Asteraceae family, to treat skin and general diseases, with Echinops kebericho being an endangered plant important in their practices.

Post-COVID symptoms are common, affecting over half of the participants.