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An elderly woman's upper lip lump, thought to be a mucocele, was actually a rare type of lymphoma usually found on legs, treated successfully with chemotherapy and radiation.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Scarring alopecia involves increased immune cells and specific gene changes near damaged hair follicles.

Hair loss gene linked to prostate issues.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

Male-pattern baldness has a weak link to heart disease and some related health conditions.

The microenvironment affects the behavior and survival of melanocytes with the GNAQ oncogene in melanoma.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

Melanocyte stem cells hold promise for skin regeneration and treating pigmentation issues.

Loss of the Y chromosome and UTY gene activity increases cancer risk in men.

Patients with severe active alopecia areata have lower CD200 expression and an imbalance in their immune system.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

HHV-6 reactivation may be linked to psychiatric disorders and can improve with antiviral treatment.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

lncRNA MTC affects protein levels in goat skin cells, impacting hair growth.

A rare skin condition with cysts was found on a 5-year-old boy's scalp.

Enhancing immune response can improve cancer treatment effectiveness.

Chemotherapy reduces splenic melanin in mice.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Alpha-MSH affects mitochondrial function, and MC1R mutations may increase skin aging.

Palmitoyl tetrapeptide-20 may help reduce hair greying and increase melanin production.

MESTSV is a rare tumor that is mostly benign but needs long-term monitoring due to potential recurrence.

Small molecules KY19382 and KY19334 may help treat skin cancer by reducing CDK1 levels and blocking harmful cell signals.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Certain MC4R gene variants are linked to higher BMI in obese women with PCOS but do not cause PCOS.

A woman had meningitis caused by mixed connective tissue disease, not an infection.

TEC kinases may help cause inflammation in vitiligo and could be targeted for treatment.