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Using cheek skin and cartilage grafts for nose reconstruction after skin cancer surgery can maintain shape and function but may require multiple surgeries and hair removal in men.

Removing Mediator 1 causes teeth cells to turn into hair cells.

A young girl developed unusually long eyelashes with a hair loss condition without other health issues or medication causes.

Disrupted stem cell signals in hairpoor mice cause hair loss.

The Foxn1 gene is essential for normal nail and hair development.

Human hair matrix cells and dermal papilla fibroblasts can form early hair follicle structures but don't produce hair shafts yet.

Secreted inhibitors of Wnt and IGF signaling control hair and tooth development, creating species-specific patterns.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

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

Genetic defects in the Wnt/PCP pathway may cause congenital yellow nail syndrome.

A Korean girl developed kinky hair without known cause or effective treatment.

Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

A woman developed rare, unexplained curly hair on her scalp and eyelashes.

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

Gentle hair care and some medications can help manage hair shaft disorders, but no specific treatment exists for congenital issues.

Children with loose anagen hair have easily pluckable hair due to root sheath problems, and it might improve without treatment.

Trichoscopic examination is crucial for diagnosing congenital triangular alopecia.

The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.

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

Three dogs with a rare skin condition improved with treatment.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

A gene mutation in mice causes severe skin disorder similar to a human condition.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Endoscopy-assisted surgery for craniosynostosis showed excellent outcomes with minimal complications and most patients went home the day after surgery.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Alopecia areata may involve disrupted mesenchymal function in hair follicles.