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Some skin problems can be signs of diabetes or other metabolic diseases and recognizing them can help diagnose and treat these diseases early.

Women with PCOS have a higher chance of experiencing depression, anxiety, and sleep disorders.

Skin problems can indicate different diseases inside the body.

Inflammation may cause nail issues in Cronkhite–Canada Syndrome.

Two sisters with lipoedematous scalp suggest a genetic influence in the condition.

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

Skin diseases like psoriasis, lupus, and others can increase heart disease risk due to factors like chronic inflammation and genetic susceptibility.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

Psoriasis patients did not show more brain atrophy or small vessel disease than controls, but longer psoriasis duration was linked to more brain atrophy.

Kindler Syndrome shows diverse symptoms and needs better diagnostic tools and care in resource-limited areas.

Dermatologists often suffer from neck, shoulder, and back pain due to their work.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

A 3-year-old girl with skin mast cell buildup and congenital baldness improved with treatment, suggesting a rare link between these conditions.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Certain factors like being female, having high cholesterol, using Medicaid, and previous non-biologic treatments increase the risk of multiple biologic failures in psoriasis patients.

Most spinal cord injury patients in Korea experience skin problems, especially fungal infections and eczema, affecting their quality of life.

Skin problems like psoriasis and systemic sclerosis can increase the risk of heart disease, so doctors should watch for heart risks in patients with these conditions.

Chronic granulomatous disease may be linked to developing systemic lupus erythematosus.

Managing multiple autoimmune diseases in one patient is very challenging.

Parry–Romberg Syndrome can involve the brain even without obvious symptoms, and a new diagnostic framework is suggested for early detection.

Three molecular subtypes of advanced skin T-cell lymphoma were identified, with potential biomarkers for predicting treatment response and disease progression.

People with Down's syndrome often have more skin problems due to a weak immune system.

Cronkhite-Canada syndrome can be diagnosed without gastrointestinal polyps if there is severe mucosal atrophy and edema.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

Steroid treatment greatly improved the symptoms of a boy with a rare disorder called Satoyoshi syndrome.

A girl initially thought to have a psychiatric disorder was later found to have a lupus-related condition, which improved with proper treatment.

Patients with Systemic Sclerosis have much higher levels of GDF-15, which could help predict organ involvement and guide treatment.

Polycystic Ovary Syndrome (PCOS) is a complex disorder with both immediate and long-term health effects, including menstrual issues, infertility, and increased risk of diabetes and heart disease.

Neuromyotonia and morphoea can occur together in the same body areas.