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The study concludes that Twenty-nail dystrophy is more common in boys among children and in women among adults, with varying response to treatment.

Regulatory T cells protect hair follicle stem cells by maintaining immune privilege in the skin.

Hidradenitis suppurativa tunnels worsen the disease and often need surgery because current treatments are not very effective.

Intralesional triamcinolone effectively reduces pain and inflammation in hidradenitis suppurativa flares.

IL-36α helps grow new hair follicles and speeds up wound healing.

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.

Early diagnosis and treatment of nail and skin conditions can improve health and appearance.

FDA-approved low-level light/laser therapy devices can significantly increase hair density in people with pattern hair loss.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Telogen effluvium is a condition that causes temporary hair loss due to stress or shock to the body.

Telogen effluvium is a type of hair loss that happens when stress or illness causes many hairs to enter the resting phase and fall out.

An 11-year-old girl with compulsive hair pulling was successfully treated with therapy and medication.

Neurotrophins regulate nerve growth by balancing promotion and suppression.

The BASP classification is more reliable than the Norwood-Hamilton for classifying hair loss in men and women.

Hormone therapy can improve sexual health and quality of life for women 70 and older.

Neonatal nasal injuries can heal with basic care but often leave scars.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Tocilizumab treatment was associated with significant hair regrowth in one patient and temporary hair loss followed by regrowth in another.

Wnt and SHH signals together influence hair follicle cell development, offering insights for hair loss treatment.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Prompt diagnosis and treatment of hair tourniquet syndrome involving the uvula are crucial to prevent severe complications.

The improved algorithm enhances low-dose CT image quality significantly better than other methods.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Hair loss common in Norwegian men, affecting self-esteem and life quality.

Nitroglycerin can stop scalp necrosis during hair transplant surgery.

Some medications for inflammation can cause a condition with scalp rashes and hair loss, often linked to Crohn's disease, and may require treatment changes to prevent permanent hair loss.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

TTD hair is brittle due to fewer sulfur amino acids and unstable disulfide bonds.

Telocytes have potential in therapy and tissue regeneration, but challenges in identification and cultivation remain.