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A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

A new gene mutation causes long hair in some Maine Coon cats.

A new type of alopecia areata, called the "confetti variant," causes small bald spots that often heal on their own in a few months.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Genetic mutations linked to ectodermal dysplasias and hair loss were identified in Pakistani families.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Removing both KLK5 and KLK7 proteins can prevent death and skin issues in Netherton syndrome.

Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

Leptin, a hormone, is important for starting hair growth.

5-alpha reductase deficiency leads to male sexual development issues and treatments like finasteride help with prostate enlargement and hair loss.

Targeting EGFR may help reduce hair loss from chemotherapy.

The monkey's hair loss was due to an autoimmune disease, not genetics.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Rice bran oil extracted by supercritical CO2 is considered non-genotoxic.

Spironolactone might lower the chance of getting rosacea.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

Intravenous calcium therapy is a safe and effective treatment for a rare type of rickets.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

PRP treatment can safely improve short-term vision in acute NAION patients.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

The CORIN gene variant causes the golden color in Siberian cats.

The KRTAP27-1 gene variations in sheep may affect wool length and weight.

Forensic genetics can now predict physical traits and lifestyle habits, with future advancements expected from new technologies.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

A gene mutation causes curly hair and hair loss in rats.

TMPRSS2 affects COVID-19 severity and treatment options.