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Tinea capitis is increasingly common in elderly women and requires accurate diagnosis with fungal cultures for effective treatment.

Tinea capitis can be misdiagnosed as bacterial infection in adult women but is treatable with antifungal medication.

DHT inhibition may increase spinal bone growth in ankylosing spondylitis.

Spiny keratoderma is a rare skin condition with small spines on palms and soles, possibly linked to abnormal hair formation.

Tinea capitis in older adults is often misdiagnosed but can be effectively treated with antifungal therapy.

Enlarged sweat gland ducts may indicate scarring hair loss.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

A woman with breast cancer developed a rare condition causing excessive fine hair growth on her face and body.

Most patients with acquired hypoparathyroidism after neck surgery had hair, nail, and skin issues.

Forehead lifting can restore a youthful look and improve brow aesthetics using various surgical and nonsurgical methods.

Acne keloidalis nuchae causes scarring on the scalp, mainly in African American males, and early treatment is important to prevent lasting damage.

A woman's severe male hormone excess was caused by a small, hard-to-find ovarian tumor.

Too much thymosin beta4 causes weird teeth and more hair growth in mice.

An adult had a rare scalp infection in the forehead area, treated successfully with itraconazole.

Primary cicatricial alopecia significantly reduces life quality, mainly due to pain and anxiety.

Temporal hair loss relates to overall scalp hair loss in women.

Primary essential CVG is a rare, benign scalp condition with treatment focusing on symptom management and hygiene.

Early diagnosis of PSIS can lead to normal height with growth hormone and testosterone treatment.

RANKL is crucial for bone health, immune function, and other body processes.

Tinea capitis can affect mental health, but treatment improves both health and well-being.

A man developed rare complications after nose surgery, stressing the need for better prevention.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

Overexpressing noggin in mice causes severe osteoporosis.

FPHL is a common, age-related, genetic hair loss with unclear causes and limited treatment options.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

Children's hairlines change shape as they grow, with women often developing a widow's peak and men's hairlines becoming more convex and possibly balding at the temples, influenced by genetics and hormones.

A rare skin condition usually found near the eyes was found on a farmer's scalp.

Forehead reduction surgery can fix forehead defects and improve appearance.

Excessive sun protection might contribute to frontal fibrosing alopecia.