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Dysregulated lipid metabolism may play a role in male pattern baldness.

A rare ovarian tumor was found in a young woman with a genetic fat disorder.

CEFFE injections effectively and safely improve postinflammatory hyperpigmentation.

Targeting cholesterol, fatty acids, fibrosis, and mast cells may help treat CCCA.

IFAP syndrome is a rare genetic disorder causing skin, hair, and eye issues, with limited treatment options.

Liposomes with minoxidil and PEP penetrate skin slowly but reach deeper layers than foam.

PLDζ2 and NPC4 have different roles in lipid changes and root hair growth in Arabidopsis under low phosphate, with PLDζ2 reducing root hair growth and NPC4 promoting it.

Policosanol biorefining shows promise for heart health, needing better academic-industrial collaboration.

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.

Doctors should consider comedonic discoid lupus erythematosus to avoid misdiagnosis.

C4BPA protein may link acne severity and insulin resistance.

A Japanese man with rare skin conditions improved with hydroxychloroquine treatment.

The Fas/FasL pathway may play a role in alopecia areata.

The new drug delivery system improves bicalutamide skin retention for better treatment of hair loss.

EGCG shows strong electron transfer interactions when bonded to DPPG lipids.

Cholesterol-related compounds can stop hair growth and cause inflammation in a type of scarring hair loss.

Lupus panniculitis of the scalp causes linear hair loss and needs ongoing treatment to prevent recurrence and lupus.

Two patients with lupus had an unusual type of hair loss not typical for the disease.

Certain fats in the skin help control inflammation and health, and changing these fats through diet or supplements might treat skin inflammation.

Platelet-rich plasma may successfully treat lichen planopillaris, as shown by one patient's symptom regression.

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

The Ysc84/SH3yl1 protein family is important for cell movement and the process of taking in materials by interacting with actin and cell membranes.

Coenzyme Q10 in nanocarriers improves treatment for hair loss.

Mycophenolic acid effectively improved hair and nail growth in a lupus patient.

Ceramide Synthase 4 is crucial for healthy skin barrier function.

CARASIL can cause different symptoms even with the same genetic mutation.

Drugs targeting EMT molecules show promise for treating lichen planopilaris.

A man with severe leprosy developed painless ulcers and numbness, treated successfully with multiple drugs and vitamins.

Liposomes with butterfly pea extract and clove oil are stable and effective according to users.