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Nonobese, normotensive Indian women with PCOS may have a higher risk of heart problems linked to inflammation and insulin resistance.

LIPH mutations cause woolly hair in some Chinese people.

The document reports the first case of a rare skin condition in Colombia, the 19th case worldwide.

Lipids are crucial for maintaining hair structure and health.

Modified HDL can better deliver drugs and genes, potentially improving treatments and reducing side effects.

Children with classic congenital adrenal hyperplasia have thicker heart fat and more heart and blood vessel risk factors, especially if their condition is not well-controlled.

Manage women's cholesterol with diet, exercise, and careful treatment choices, especially during pregnancy, PCOS, and menopause.

Lichen planopilaris involves disrupted fat metabolism, increased scarring, and mast cell activity.

Dermoscopy helps diagnose rare GLPLS in males.

ECCL should be considered in patients with specific skin and eye lesions.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Men with male pattern baldness may have a higher risk of heart disease due to increased levels of a specific lipid in their blood.

A rare scalp condition caused scarring hair loss in a woman, improved slightly with treatment.

A boy had a rare scalp condition with thickened skin and different-colored hair.

A sphingolipid from human placenta may help treat vitiligo by activating melanocyte stem cells.

Cicatricial pattern hair loss is likely advanced common baldness, not a type of lichen planopilaris.

SCD1 inhibitors can cause skin issues in rodents.

Clim proteins are essential for maintaining healthy corneas and hair follicles.

A woman with lupus had right heart failure due to blood clots in her lungs, but treatment improved her condition.

A woman with lupus had blood cell destruction, treated successfully with medication.

Phospholipase A2 enzymes play key roles in skin health and disease.

Two sisters with lipoedematous scalp suggest a genetic influence in the condition.

Children with classic congenital adrenal hyperplasia have thicker heart fat and are at higher risk for heart problems and early atherosclerosis.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

GLPLS and LPP are variants of lichen planus.

Liposomes could improve how skin care products work but are costly and not very stable.

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.

Different sPLA2 enzymes have unique roles in phospholipid metabolism and biological processes.