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TB lymphadenitis can occur in people with weakened immune systems, like those with SLE.

Early recognition and treatment of LPP can prevent hair loss and improve quality of life.

A 4-year-old girl had a rare hair disorder affecting only part of her scalp.

JSLE patients often have more hormone and metabolism issues, so regular check-ups and preventing obesity can help.

Timely and aggressive treatment is crucial for improving outcomes in severe complications of adult-onset Still's disease.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Early diagnosis and coordinated care are crucial for managing lupus effectively.

A young woman with lupus was treated with hydroxychloroquine and prednisone.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

Cadd4 effectively reduces cholesterol levels without side effects.

Laser skin treatments can lead to viral infections like molluscum contagiosum, so precautions are important.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

Glucocorticoid treatment in lupus can cause oral lesions, which need early diagnosis and comprehensive care.

Deleting the CDSN gene causes severe skin and hair problems, leading to death.

The ESLD recommends international safety guidelines and standards for home-use light-based hair removal devices.

Hormonal changes and social stress may link lupus and eating disorders in teens.

A man with Cronkhite-Canada syndrome had all 20 nails detach but improved with treatment.

PCFCL may have unrecognized subtypes and needs more research.

TB lymphadenitis can occur in people with weakened immune systems, like those with SLE.

CCCA is a common, progressive hair loss condition that may not always be linked to hair care practices and requires a biopsy for diagnosis.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Choosing the right tools is crucial for accurately measuring lupus activity and damage.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Taiwan reported its first case of a rare scalp condition with no clear cause or treatment.