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A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

A specific gene mutation causes woolly hair and hair loss.

A mutation in the KRT74 gene causes tightly curled hair.

Mutations in the SNRPE gene cause hereditary hair loss.

A mutation in the KRT25 gene causes woolly hair and hair loss.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Genetic hair shaft abnormalities can be seen with microscopes and often affect scalp hair.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

A 19-month-old boy with a rare hair disorder showed mild improvement with treatment, but his family chose gentle hair care due to limited success.

Local hairline measurements are important for better surgical results and early disease detection in Colombian women.

A mutation in the KRT75 gene causes frizzle feathers in chickens.

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

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

PCOS is likely inherited in families, increasing risk for first-degree relatives.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Frontal Fibrosing Alopecia's cause is unclear, affects mainly postmenopausal women, and current treatments focus on stopping hair loss rather than regrowth.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

More research is needed to better understand and treat Fibrosing Frontal Alopecia.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.