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Certain gene variations may protect against skin issues and oxidative stress in women with PCOS.

New mutations in the DSG4 gene cause a rare hair condition.

Stem cell therapy shows promise for treating skin issues in animals.

Hidradenitis suppurativa is linked to various diseases like obesity, depression, arthritis, and Crohn's disease, but often occurs alone.

Late dumping syndrome after fundoplication can be diagnosed with an oral glucose tolerance test and managed with diet changes.

Trichodysplasia spinulosa is a rare skin disease in immunocompromised patients caused by a specific virus targeting hair follicle cells.

Ultrasonography in dermatology improves diagnosis and treatment of skin conditions.

People with seborrheic dermatitis often have lower vitamin D levels.

CO₂ laser surgery successfully healed a dog's chronic paw condition.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

KID syndrome should be reclassified as an ectodermal dysplasia.

A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.

Graft-versus-host disease occurs when donor immune cells attack the recipient's body, causing skin, gut, and liver damage.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Spontaneous keloids may be linked to nephrogenic systemic fibrosis in dialysis patients.

Hypospadiac rats showed abnormal genital development, useful for studying human hypospadias.

Severe digestive issues in DRESS need early endoscopy for better treatment.

Higher DHEA-S levels are linked to smaller ovarian volume in women with PCOS.

A 72-year-old man was diagnosed with a rare skin form of Rosai-Dorfman disease after years of misdiagnosis.

PEODDN is a rare skin disorder with limited treatment options, best treated with laser therapy.

Skin changes during pregnancy are common, and non-invasive imaging is safe for monitoring these changes.

A patient with a scalp condition and benign skin tumor experienced hair loss and did not improve with treatment, choosing not to have surgery despite a small cancer risk.

Vascular endothelial cells may significantly influence skin stem cells, but more research is needed.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

The authors suggest standardizing how the heart's electrical axis is calculated to improve precision and consistency in ECG analysis.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

The document reports a rare case of ECCL with a new association with optic disc colobomas.