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A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21, near the hairless gene.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

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

5% topical minoxidil can significantly improve hair growth in children with Marie Unna hereditary hypotrichosis.

Topical minoxidil may help improve hair growth in rare congenital hypotrichosis.

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

A hair growth ointment improved hair length in a family with a genetic hair growth condition.

Girls with prepubertal simple hypertrichosis have higher dihydrotestosterone (DHT) levels.

Localized hair growth and fat loss may share a common cause in lupus panniculitis.

Some burn patients grew extra hair in areas treated with pressure garments or silicone.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

A girl inherited excessive body hair from her mother and grandmother.

Long-term repeated cupping therapy can cause unexpected localized hair growth.

A miner developed extra shoulder hair due to long-term work pressure and inflammation.

Increased hair growth after a cast is temporary and harmless.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Prolonged UVB exposure causes significant skin changes and damage in rats.