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Researchers found that certain lipids, especially vitamin D3, are lower in prematurely grey hair than in pigmented hair.

A test for nail fungus was most accurate with PAS stain, low-dose spironolactone helped two-thirds of acne patients, metformin reduced symptoms of HIV-related fat distribution changes with some side effects, and skin examination with dermoscopy was better at detecting abnormal moles, while temporary tattoos can cause skin reactions.

New hair after alopecia areata can be thinner and change color but usually keeps the same shape.

The hamartoma is an abnormal hair growth with limited development in the upper hair follicle.

Dermatologists should recognize diverse discoid lupus signs to avoid misdiagnosis.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

Triamcinolone is more effective and safer for treating feline pemphigus foliaceus than prednisone.

A woman's rare hair loss condition improved on its own, suggesting this type might recover like common cases.

Human dermal stem cells can become functional skin pigment cells.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

Linear lichen planopilaris can affect the trunk, not just the face.

A 5-year-old girl with a rare skin disorder was effectively treated with skin creams instead of oral medication.

Brown skin in guinea pigs has more ascorbic acid and related enzymes, black skin uses ascorbic acid well, and white skin has the most protein.

Hair diameter difference, brown skin discoloration around hair follicles, and missing hair in certain areas are key signs of androgenetic alopecia (commonly known as hair loss) when viewed under a dermoscope.

A single long white eyelash is a rare but benign condition.

LC-OCT is a promising tool for diagnosing and monitoring Alopecia areata.

UV dermoscopy helps detect white hairs in children more effectively.

An 8-year-old girl developed a rare skin condition in a linear pattern on one side of her body after a lung infection, which improved with treatment.

Spanish speakers with limited English search most for "pigmentation/dark spots."

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

A rare hair follicle disorder can cause itchy, bluish-black bumps on the body.

Spiny keratoderma may be ectopic hair formation on palms and soles.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

The patient improved significantly after treatment, with only one small scar remaining.

A 54-year-old woman experienced progressive hair loss starting in adolescence, leading to sparse scalp hair and almost no eyebrows or eyelashes.

A rare scalp infection in a child developed into a kerion with additional skin symptoms.

Thorough hair examination is crucial for accurate diagnosis and treatment.

A young Caucasian man experienced a rare type of hair loss on the back of his head.

A 7-year-old girl was diagnosed with Netherton's Syndrome, shown by skin and hair symptoms.

The study found specific hair and scalp patterns for different types of hair loss in Koreans, noting racial differences affect diagnosis.