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A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Localized hair growth and fat loss may share a common cause in lupus panniculitis.

Hyperaesthetic leucotrichia in horses causes painful, recurring skin lesions and hair color changes, especially in Arabian and American paint horses.

Severe CCCA may be biologically and clinically different from milder forms.

A 38-year-old man was diagnosed late with Kearns-Sayre syndrome after being wrongly treated for epilepsy.

The document found differences in lesion distribution and microscopic features among trichostasis spinulosa and similar skin conditions.

TB can mimic SLE symptoms, so doctors should consider TB in such cases.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

A woman with a rare scalp condition causing a thick scalp and hair loss didn't improve with steroid treatment.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

The newborn was diagnosed with a rare skin disorder causing blisters, which requires careful wound care and family support.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

Facial lichen planopilaris may be triggered by shaving and mustard oil, and early detection is crucial for better treatment outcomes.

Early diagnosis and a multidisciplinary approach are key to managing Sjogren's Disease symptoms.

Early detection and treatment of primary biliary cirrhosis and related autoimmune diseases improve outcomes.

A gene mutation in mice causes severe skin disorder similar to a human condition.

A baby had a rare condition with abnormal blood vessels in the brain and unusual skin and hair growth, possibly a new syndrome.

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

EGFR and mTOR inhibitors may help manage Olmsted syndrome symptoms.

CLASI is a valid tool for assessing skin activity and damage in lupus patients.

Treatment with vitamin A did not improve the child's skin condition.

CD4+ lymphocytopenia can occur in patients with systemic lupus erythematosus.

Autoimmune polyglandular syndrome can cause temporary brain issues that may improve on their own.

COVID-19 may trigger systemic lupus erythematosus, requiring careful diagnosis and treatment.

Obesity is linked to various skin disorders, which can help with early diagnosis and prevention of long-term health issues.