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Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

External factors can cause skin cancer cells that usually don't spread to grow and form tumors in mice.

Pets in Egypt can pass skin fungus, especially Microsporum canis, to humans, with outdoor and young pets being more at risk.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

LncRNA018392 helps goat skin cells grow by increasing CSF1R.

Isolated patchy heterochromia with pili annulati can occur without other health issues.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

Itraconazole is effective for treating scalp ringworm, and a Wood's lamp is a useful diagnostic tool.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

New treatments for hair growth and psoriasis may be possible, and gene differences could affect baldness and the severity of skin conditions.

Mutations in the DSG4 gene cause specific hair and scalp issues.

Researchers found that certain miRNAs, which affect immune system regulation, are differently expressed in mice with a hair loss condition compared to healthy mice.

COVID-19 may harm male fertility by affecting sperm production.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Two microRNAs affect hair follicle development in sheep by targeting specific genes.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Psoriasis patients did not show more brain atrophy or small vessel disease than controls, but longer psoriasis duration was linked to more brain atrophy.

The study explores miRNA changes in female hair loss.

The study explores miRNA changes in female hair loss.

Keratin mutations may cause scarring alopecia by damaging hair structure.

A woman with myotonic dystrophy had multiple skin tumors on her scalp, suggesting a genetic link.

A 17-year-old girl has had repeated hair loss since childhood, which can be triggered by infections like COVID-19.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

Cyclosporine effectively treated a woman's stubborn skin condition.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.