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A rare combination of halo nevi, nonsegmental vitiligo, and early gray hair can occur together.

Recognizing the "bamboo hair defect" is crucial for diagnosing Netherton's syndrome.

Pigmentary mosaicism causes skin color changes and can affect multiple body systems, but has no cure.

Ectopic acanthosis nigricans can occur at surgical sites due to skin graft mismatches.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

Newborns with hair loss and red, scaly skin need thorough skin checks to find the cause and treatment.

Early recognition and evaluation of nevus sebaceus are crucial to detect and manage potential cancerous changes.

The patient has a rare skin condition that shows features of two known disorders.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps from birth.

A 4-year-old girl has a rare condition causing hairlessness and skin bumps, but normal teeth and sweating.

A 16-year-old boy had a rare case of Becker's nevus on his face and mouth.

The study concluded that a 'Swiss cheese' pattern in hair follicles is a useful sign for diagnosing alopecia areata.

The study found unique skin changes in a rare type of alopecia linked to a skin condition called linear morphea.

Nevus comedonicus is a rare skin condition causing dark bumps, treatable with retinoic acid or surgery.

Orange spots in scalp trichoscopy can help diagnose scalp sarcoidosis.

Dermoscopy helps diagnose and monitor treatment for hair loss from scarring conditions like discoid lupus and lichen planopilaris.

A new type of alopecia areata, called the "confetti variant," causes small bald spots that often heal on their own in a few months.

Some families have a genetic condition where they are born with irregular scalp defects.

A 16-year-old boy's facial condition improved with doxycycline, suggesting an immune response to hair follicle damage.

A 17-year-old in Saudi Arabia was diagnosed with a rare skin condition causing red-brown facial patches.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.

Shiny white structures in trichoscopy can indicate long-standing discoid lupus erythematosus alopecia.

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

CCCA is a common, scarring hair loss in Black women that needs early detection.

A child with a rare scalp condition regrew hair after treatment.

CCCA causes progressive hair loss in Black women, starting from a central scalp patch.

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

The boy's hair fully regrew after treatment for a rare hair loss condition.

A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

Chronic cutaneous lupus erythematosus causes scarring, hair loss, and skin discoloration, especially on sun-exposed areas.