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TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

Addressing underrepresentation in Parkinson's research is crucial for better treatments and understanding.

Air Vice-Marshal Sir Ralph Jackson significantly advanced dialysis technology in the UK.

People distressed by minor skin changes should consult dermatologists with cosmetic expertise, and a public Cosmetic Dermatology Service with mental health support is recommended.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

Symmetrical Acrokeratoderma (SAK) may be a unique skin condition in China, lacking specific treatment and needing long-term monitoring.

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.

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.

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.