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People with psoriasis are more likely to have Metabolic Syndrome than those without psoriasis.

Steroid treatment improved both gut and nerve symptoms in a man with Cronkhite–Canada syndrome.

Clouston syndrome can lead to skin cancer, so monitoring is crucial.

There is no standard treatment for the rare Cronkhite–Canada syndrome, which can be fatal and lead to cancer.

The case shows how hard it is to tell apart Multiple Autoimmune Syndrome from other similar autoimmune conditions, but correct diagnosis is key for treatment to work.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

Patients with metabolic syndrome often have skin problems like acanthosis nigricans and skin tags, and early treatment is important to prevent serious issues.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

Recognizing and managing skin-related psychiatric disorders in children is crucial for effective treatment.

People with certain skin disorders are more likely to have alcohol problems, especially if they also have mental health issues like depression and anxiety.

The new classification system for skin disorders emphasizes the importance of understanding a patient's awareness of their condition for better treatment.

A 60-year-old man with Cronkhite-Canada syndrome improved with treatment, but the condition has a high mortality rate and a risk of colorectal cancer.

Many skin patients have mental health issues, but few dermatologists are well-versed in treating these conditions.

Merkel cell carcinoma is most likely to recur within two years of diagnosis, and factors like immune suppression, being over 75, and male sex increase this risk.

Early diagnosis and nutritional support are crucial for managing Cronkhite-Canada Syndrome.

Corticosteroids improved symptoms in a man with Cronkhite-Canada Syndrome.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

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

Primary mitochondrial cytopathies often cause skin, endocrine, vision, and blood issues, needing careful diagnosis.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

Skin and mucous symptoms are key for diagnosing autoimmune connective tissue diseases.

The report described a unique case of Cronkhite-Canada syndrome with unusual polyps and an association with multiple myeloma.

Cronkhite-Canada syndrome is a rare, non-inherited condition causing various symptoms like polyps, hair loss, and weight loss.

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

Certain factors can trigger hormonal imbalances and cyst formation, leading to Polycystic Ovarian Syndrome (PCOS).

Children with different rheumatologic diseases have specific skin symptoms that can help with diagnosis.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.