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Severe CCCA may be biologically and clinically different from milder forms.

Necrobiosis lipoidica may need new criteria for accurate diagnosis due to similarities with another condition.

Two new gene mutations cause a rare hair disorder.

Human body's immune cells are more common in the layer of fat just beneath the skin than in deeper fat layers.

Low vitamin C caused bleeding and corkscrew hair, resolved with vitamin C treatment.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Women with PCOS have overall higher body fat, not abnormal fat placement, and more insulin resistance.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

Hair manganese may relate to cardiometabolic health, not coronary artery disease severity.

Alopecia can be caused by multicentric reticulohistiocytosis.

Targeting lipid metabolism can help treat advanced, resistant cancers.

A 13-year-old boy with Cushing syndrome has high cortisol levels from a pituitary gland issue and underdeveloped sexual characteristics.

Cronkhite-Canada syndrome is a rare condition causing gut polyps, hair loss, skin changes, and nail issues, often with a poor outlook.

Obese and non-obese women with PCOS have higher heart risk markers, especially if they are obese.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

A 36-year-old man had unusual skin lesions on his face without hair loss.

The Flo app showed that bloating, high cholesterol and glucose levels are common in women with Polycystic ovary syndrome (PCOS), and these symptoms increase with body mass index (BMI), suggesting a need to refine PCOS diagnosis criteria.

Steroid treatment improved both gut and nerve symptoms in a man with Cronkhite–Canada syndrome.

Targeting glycolysis may help treat PCOS by improving insulin sensitivity and ovarian function.

A specific genetic mutation causes POMC deficiency, leading to symptoms like weight gain and red hair.

Thrombophilic conditions may worsen Long COVID symptoms due to increased blood clotting.

Women with PCOS in Nigeria have higher heart risk markers, needing early heart health checks.

Mutations in the KRT85 gene cause hair and nail problems.

Sca-1+ cells in newborn mouse skin may become fat cells.

Reflectance confocal microscopy can noninvasively diagnose onychomatricoma by showing unique features different from healthy nails or nail fungus.

The LMNA mutation affects skin structure even in asymptomatic carriers.

Women with the NIH type of PCOS have more obesity and higher risk of diabetes and heart disease than those with other types of PCOS.