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A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

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

Hair loss in androgenetic alopecia is caused by genetic factors and androgen excess, and can be treated with combined therapies.

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

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

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

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

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

Loose Anagen Hair Syndrome is a hereditary condition causing hair loss in children due to abnormal hair follicles.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

Eruptive vellus hair cysts are a cosmetic skin condition, more common in young adults, with few effective treatments.

Some families have a genetic condition where they are born with irregular scalp defects.

Loose Anagen Syndrome causes easy-to-pull, thin hair, mainly in young girls, and improves with age.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Pseudopelade is a rare inherited hair loss condition with a genetic cause.

An 18-year-old girl was diagnosed with a rare hereditary hair loss condition, despite no family history.

Monilethrix is a rare genetic hair disorder that's hard to treat.

Short Anagen Syndrome causes persistently short hair and increased shedding, usually improving after puberty.

Selective breeding caused the unique curly hair in Mangalitza pigs.

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

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

A woman's hair changed to a dry, tangled texture that's hard to comb after treatment with spironolactone, suggesting the medication might cause such hair changes.

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

Porphyria cutanea tarda causes skin issues due to an enzyme deficiency.

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

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

The document explains the genetic causes and characteristics of inherited hair disorders.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.