Search

everythinglearnresearchcommunity

for

Search:↓

Localized dystrophic epidermolysis bullosa (DEB) can lead to scarring alopecia, highlighting the need to recognize and address this complication.

A woman with Parry-Romberg syndrome developed new curly hair on one side of her scalp, a condition not previously linked to the syndrome.

Facial trichostasis spinulosa is a chronic condition with significant cosmetic impact, especially in young women.

Netherton's disease causes multiple hair defects.

Better diagnostic tools and treatment guidelines are needed for segmental vitiligo and related pigment issues.

Most Korean systemic lupus erythematosus patients experienced hair loss, often as non-scarring diffuse hair loss, with non-scarring patch alopecia also common.

Catatonia can be a rare sign of lupus, needing careful diagnosis and treatment.

The flaky skin mouse mutation is a natural model for studying human psoriasis.

Mutations in the DSG4 gene cause specific hair and scalp issues.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Systemic lupus erythematosus is an autoimmune disease causing diverse symptoms and major organ involvement.

A 17-year-old girl with Kartagener's syndrome also has unusual skin, hair, and nail issues.

SQSTM1 is linked to increased risk of alopecia areata.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

A patient had both chronic lupus and systemic scleroderma, requiring careful treatment to manage symptoms.

Seborrheic dermatitis affects quality of life and sleep, linked to stress and nervous system changes.

Trichoscopy can reveal specific hair and scalp changes in linear morphea.

Dermoscopy is useful for accurately diagnosing syphilitic alopecia.

A gene deletion in DSG4 causes sparse hair in some Pakistani families.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

New hair and skin changes were found in a rare case of syphilis-related hair loss.

PEH in vulvar LS is common and needs careful diagnosis to avoid confusion with cancer.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Trichoscopic patterns often overlap in scalp disorders, so dermatologists need to stay updated.

Olmsted syndrome is a rare skin disorder causing thickened skin and other symptoms.

Ustekinumab treatment may reveal a genetic tendency for steatocystoma multiplex in psoriasis patients.

SLE should be considered in horses with immune-related skin issues.

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.