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Brow lifts raise and smooth the forehead and can lower the hairline.

A woman with a rare ovarian tumor and hyperparathyroidism improved after surgery, highlighting the need for reporting unusual cases to understand and manage rare diseases.

The girl has a hormonal imbalance causing increased hair growth and other male characteristics.

Lupus can be a rare cause of high calcium levels in the blood.

Older women taking spironolactone for hair loss may need yearly potassium checks due to a higher risk of hyperkalemia.

Soft-tissue calcification is rare in systemic lupus erythematosus.

Becker's Nevus Syndrome is a rare condition with a skin patch and possible bone and muscle abnormalities, treated mainly for appearance.

A rare scalp condition, cutis verticis gyrata, was found in a woman with primary scarring alopecia.

A six-year-old girl with extra hair on her elbows was treated with hair removal methods.

The gene Prss53 affects hair shape and bone development in rabbits.

KFSD causes scarring hair loss and skin roughness, mainly in males.

Better diagnostic and treatment strategies are needed for acne keloidalis nuchae, especially in high-risk groups.

JOLT uses fillers to lift and tighten the lower face and neck.

The new system helps detect and track early female hair loss better.

Acne keloidalis nuchae is a hair loss condition affecting men of African descent, causing scar-like bumps on the scalp and neck.

9-cis-retinoic acid showed some effectiveness in treating AIDS-related Kaposi sarcoma but had significant side effects at higher doses.

A woman experienced temporary hair loss after jaw surgery, which can be reduced by careful head positioning during the operation.

β-interferon injections for melanoma can cause excessive hair growth at the injection sites.

KGF and its receptor are found in enlarged prostate tissue and KGF strongly increases cell growth.

A 70-year-old man with skin cancer on both sides of his forehead was treated with surgery and cryotherapy, highlighting the need for early detection and prevention.

The man had pretibial myxedema and hyperthyroidism, causing skin changes and thyroid issues.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

Avoiding damage and using specific shampoo and supplements improved the hair condition.

Immature hypertrophic scars on the head and neck have more inflammation and TGF-β, affecting treatment choices.

A 38-year-old man was diagnosed late with Kearns-Sayre syndrome after being wrongly treated for epilepsy.

Leukemia can sometimes appear as unusual skin issues in children.

A postmenopausal woman's excess male hormone symptoms improved after her ovaries were removed.

The study suggests that acne keloidalis nuchae is linked to conditions like pseudofolliculitis barbae, scalp infections, metabolic syndrome, and is more common in males with an average onset age of 25.4 years.

VKHD and sarcoidosis may share a common cause.