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The Walleye dermal sarcoma virus cyclin causes excessive skin cell growth in mice.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

LGR5 and LGR6 are expressed differently in various skin tumors, which may offer clues about their origins.

Stopping methotrexate might reverse lymphoma-like conditions in some patients.

A woman with a long-term skin condition developed a serious skin cancer that led to her death.

The woman has a rare skin condition called follicular Dowling-Degos disease, which has limited treatment options.

Ossification in trichilemmal cysts is more common than previously believed.

T cell subsets are crucial in kidney cancer, and a new model predicts patient outcomes using key genes.

RET mutation is important in familial medullary thyroid carcinoma, and BRAF mutation in papillary thyroid carcinoma is linked to more aggressive cancer and higher death rates.

Trichoblastomas may mimic fetal skin development by having many Merkel cells, unlike adult skin.

A transwoman developed a brain tumor after nine years of hormone therapy, suggesting a possible link between the treatment and tumor development.

A rare skin tumor with bone formation was successfully removed without recurrence.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

GLI1 RNA CISH effectively identifies basal cell carcinoma but is less specific for benign follicular tumors.

A rare case showed basal cell carcinoma and leiomyosarcoma coexisting, needing careful diagnosis and treatment.

Wedelolactone may help prevent bone damage in breast cancer by blocking certain cell signals.

Stopping Viviscal, a hair loss product, normalized the woman's elevated alkaline phosphatase levels.

A cancer patient developed a type of hair loss after starting a cancer drug called vandetanib.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

Lifestyle factors like BMI at young adulthood can increase cancer risk in women with Lynch Syndrome, but diet and height don't seem to affect this risk.

Vogt–Koyanagi–Harada disease can cause rare hair growth on normally hairless thumb skin.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

The study concludes that Loose Anagen Hair Syndrome is a benign condition that usually improves with age but can be hard to diagnose and stressful for the family.

High LGR5 levels in glioblastoma indicate poor prognosis and are essential for cancer stem cell survival.

A woman's hair loss and other symptoms were due to a rare hormone deficiency treatable with steroids.

The tumor on the man's nose was a rare type called pedunculated follicular hamartoma.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requires high doses of calcium and vitamin D for management.

A 7-year-old girl had a non-painful skin growth at her belly button, which was removed and identified as a keratinous cyst.

Testosterone therapy improved physical and social health in a male with 49,XXXXY syndrome.

Different types of skin gland tumors have unique genetic traits, which can guide personalized treatments.