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RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

A woman experienced total hair loss after an HPV vaccine, but treatment helped regrow her hair.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

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

Follicular porokeratosis may be linked to diabetes and can lead to hair loss.

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

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Researchers found a new mutation causing total hair loss from birth.

Traumatic panniculitis can cause increased hair growth in affected areas.

Too much parathyroid hormone-related protein in skin disrupts hair growth in mice.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

Nested PCR can reliably identify fungal infections when traditional methods fail.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

A nine-year-old girl with muscle weakness and total hair loss improved with specific treatments.

A hereditary condition causes hair loss and twisted hair in some family members.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Monkeypox skin lesions show full-thickness skin death and swollen skin cells, with the virus found in affected cells.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

Linear lichen planopilaris can affect the trunk, not just the face.

HTLV-1-associated lichenoid dermatitis (HALD) is linked to an immune response against HTLV-1-infected cells.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

E6/E7 oncogenes in hair follicles cause continuous hair growth by skipping the resting phase.

Immortalized human dermal papilla cells were created that grow better and can still help form hair.

The study concluded that key signs of Keratosis follicularis spinulosa decalvans are changes in terminal hair and vellus hair follicles, which likely start the inflammation and damage to hair follicles.

A young boy with a rare skin and nail condition improved significantly with simple topical treatments.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.