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Cutaneous lupus erythematosus is a common skin condition in lupus, affecting mostly young adult females.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

Digital gangrene can be a rare first sign of late-onset systemic lupus erythematosus.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

The horse had a rare disease causing weight loss and skin issues, leading to euthanasia due to poor treatment options.

Hormonal therapy is essential in late-diagnosed Kallmann's syndrome to prevent bone issues.

A medication called sodium valproate likely caused a girl's hair to become kinky and dry.

A man with rare skin changes on his fingers was diagnosed with multiple myeloma-linked amyloidosis.

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

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Woolly hair syndrome is a genetic condition causing frizzy, fragile hair.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

The European Society of Cutaneous Lupus Erythematosus created a questionnaire to standardize patient assessment and improve care for cutaneous lupus.

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

Isoliensinine, a natural compound, prevents stress-related hair greying by blocking a specific receptor on hair cells.

Autoimmune Polyendocrine Syndromes involve specific combinations of autoimmune diseases.

Two siblings have a rare hair condition caused by a new genetic variant.

The newborn's skin blistering is due to a genetic condition called epidermolytic hyperkeratosis.

Syphilis treatment resolved hair loss and eye symptoms, highlighting its importance in diagnosing unusual alopecia.

Finasteride may cause lasting sexual and mental health issues, and genetic screening could help prevent them.

Elderly SLE patients show fewer typical symptoms and more hormonal side effects.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

Early and aggressive treatment with individualized care plans is crucial for managing pediatric systemic lupus erythematosus.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

The meeting showcased rare skin disease cases, highlighting the need for accurate diagnosis and treatment.

The boy's symptoms suggest a possible new medical condition.

The Polish Dermatological Society recommends personalized treatment for cutaneous lupus, including lifestyle changes, medications, and monitoring, with specific drugs for severe cases.

The CLASI is a reliable tool for measuring the severity of cutaneous lupus erythematosus.