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The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

A new DSG4 gene mutation causes hair defects in a young girl.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

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

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

HIV-positive men who have sex with men have a higher rate of anal beta-papillomavirus infections.

A unique hair tumor with a rippled pattern was identified, showing incomplete differentiation and unusual cell arrangements.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

Mutations in the LIPH gene cause woolly hair in a child.

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.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

A young woman had a rare scalp tumor usually found in older women.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

Dengue virus can infect human hair follicle cells and may cause hair loss.

Dupilumab improved hair and skin in a woman with Netherton syndrome.

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

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

A Turkish woman has a hair condition caused by a LIPH gene mutation.

The hair disorder was caused by abnormal protein formation, making hair easily damaged.

Minoxidil use can cause trichostasis spinulosa in long-term hair loss patients.

A new type of pachyonychia congenita may exist, caused by a different keratin mutation.

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

Autoimmune myopathy may be linked to hair loss and skin depigmentation.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

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.

PAON shows skin patterns due to genetic mosaicism.

Dermoscopy is useful for diagnosing Atrichia with Papular Lesions in children without needing a biopsy.