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Intralesional chemotherapy with 5-fluorouracil and methotrexate may worsen keratoacanthoma-type skin cancer in transplant patients.

The combined treatment effectively managed severe skin issues in Olmsted syndrome.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

Biopsy is crucial for accurately diagnosing EPDS to avoid mistaking it for SCC.

Alpha-difluoromethylornithine prevents cancer in mice but causes hair loss.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

The Gsdma3 gene is essential for normal hair development in mice.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

The enzymes Tet1, Tet2, and Tet3 are important for the development of hair follicles and determining hair shape by controlling hair keratin genes.

Lack of Ctip2 in skin cells delays wound healing and disrupts hair follicle stem cell markers in mice.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Human liver enzyme DHEA ST helps process minoxidil.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

MAD2B slows down the growth of skin cells that are important for hair development by interacting with TCF4.

Mutations in the KRT16 gene can cause skin and nail disorders.

Manipulating 5α-reductase type 2 can affect liver fat production and glucocorticoid effects.

Deleting TNFα gene reduces skin cancer risk in certain mice.

Hereditary elliptocytosis causes elongated red blood cells and can lead to mild or no symptoms.

Mice without certain skin proteins had abnormal skin and hair development.

Desmocollin 1 is essential for strong skin and proper skin function.

Increased ornithine decarboxylase makes normally tumor-resistant mice more sensitive to tumors.

Targeted protein degraders show promise in treating cancer but need to target more diverse proteins.

Localized dystrophic epidermolysis bullosa (DEB) can lead to scarring alopecia, highlighting the need to recognize and address this complication.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

Keratin 10 end domains may increase skin cancer risk by reducing cell death.

Recognizing minor skin lesions can help identify serious cancer syndromes.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.