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Trichilemmal keratinization is a unique process in hair follicles where the outer root sheath turns into keratin without a specific layer.

Baricitinib may reactivate trichilemmal cysts in people with a history of these cysts.

A rare benign tumor was found in a man's scrotum, highlighting the need for accurate diagnosis.

Trichoscopy helps tell apart scalp lesions in pemphigus vulgaris and pemphigus foliaceus and is useful for choosing biopsy locations.

A child died from eating hair, causing severe stomach blockages and infection.

Dissecting cellulitis may have genetic links and can cause permanent hair loss.

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

A rare skin bump with tiny hairs was successfully removed from a man's face.

The new wound dressing helps heal abdominal wall defects faster by improving the wound environment.

A girl with Crohn's disease had a hairball causing bowel obstruction, which was removed, and she recovered well.

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

The report found a new type of hair loss in African-American women that affects more areas of the scalp than previously thought.

Applying a tretinoin cream can remove hair plugs and treat trichostasis spinulosa.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

A specific gene mutation causes complete hair loss in an Irish Traveller family.

Trichoscopy helped diagnose and treat a child's fungal scalp infection by spotting specific hair shapes.

A black pore on a man's cheek was a hair follicle tumor and was removed.

The horse had a rare type of hair loss caused by immune cells attacking hair follicles.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

Trichotillomania is a condition where people repeatedly pull out their hair, which can be triggered by stress and has various physical signs.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

Researchers found a new mutation causing total hair loss from birth.

Hair shaft malformation contributes to Central Centrifugal Cicatricial Alopecia.

Trichohyalin granules help inner root sheath cells in hair follicles harden by integrating with keratin filaments.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.