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CE-PTG is a better method for analyzing hair growth in androgenetic alopecia.

Keratoacanthoma changes as it grows, showing different hair follicle characteristics at each stage.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

The four patients have a unique type of ichthyosis affecting hair follicles.

Some skin changes from pregnancy like hair loss, excessive hair growth, palm redness, and stretch marks may not go away after birth and could suggest a misdiagnosis or hidden condition.

Peripilar keratin casts are a helpful sign for diagnosing traction alopecia.

Older people with severe COVID-19, especially those with certain health conditions, are more likely to experience post-COVID syndrome.

CTE can distort results in hair growth trials, so exclude it carefully.

Overexpressing Merkel cell virus proteins in human hair follicles can create clusters of cells that resemble Merkel cell cancer.

Hair cortisol levels can show increased stress during late pregnancy but only for up to six months.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

Trichoscopy is effective in diagnosing trichotillomania by showing specific hair patterns.

The report suggests that hair loss in Cronkhite-Canada syndrome may be caused by alopecia areata incognita, as shown by a patient's improvement with treatment.

Patients with non-scarring alopecia often experience emotional disorders like depression and stress.

The case suggests a possible link between severe acne and certain bone deformities.

Different species have unique sensory adaptations to perceive their environments.

A 32-year-old woman's hair loss was linked to skin nodules and severe headaches.

Shifting attention can reduce physical pain.

EBV infection increases a specific keratin variant in carcinoma cells, possibly affecting cell structure and cancer progression.

A 62-year-old woman got a lump on her eyelid from tiny mites, which is the first time this has happened.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

Taking photos of your own skin can lead to fewer skin biopsies for mole monitoring.

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

Long-COVID has diverse, long-term health impacts, especially in young people.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

Unexplained excessive hair growth can signal underlying cancer and often indicates a poor prognosis.

Corkscrew hair may be a new sign for quickly diagnosing scalp fungus in black children.

Type II keratins are uniquely phosphorylated during stress and mitosis, affecting their structure and function.

Too much keratin 16 in mice skin causes abnormal skin thickening and structure.