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Narrowband-UVB phototherapy successfully treated a rare case of Graham Little-Piccardi-Lassueur syndrome.

The girl's symptoms suggest a complex condition that's hard to diagnose despite normal test results.

Cri-du-chat syndrome can cause skin and oral lesions affecting nutrition and quality of life.

Satoyoshi syndrome is likely an autoimmune disease that mainly affects young women and improves with immune-related treatments.

Early recognition and a team approach are crucial for managing diffuse alveolar hemorrhage in antiphospholipid syndrome.

Diagnosing and managing Glucocorticoid Resistance Syndrome is complex due to genetic differences and varied symptoms.

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

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Early recognition and multidisciplinary management are crucial for improving outcomes in Parry-Romberg syndrome.

Pyoderma gangrenosum can occur in rheumatoid arthritis patients and may be mistaken for vasculitis.

Glucocorticoid treatment improved symptoms in a girl with Satoyoshi disease.

A woman with chronic hepatitis C had a rare skin condition linked to her illness.

Two patients with Cronkhite-Canada syndrome achieved remission after treatment.

The cause of the syndrome with scalp scaling and hair loss is unknown.

Cantú syndrome is caused by mutations in the ABCC9 gene.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

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

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

Steroid pulse therapy improved symptoms in a man with Satoyoshi syndrome.

Careful management of chronic hyponatremia is crucial to prevent severe neurological issues.

Managing multiple autoimmune diseases in one patient is very challenging.

A man developed myasthenia gravis after alopecia areata, and treatment improved his symptoms and stopped hair loss.

RCVS should be considered in thunderclap headaches, and MRA and DSA are better for diagnosis than CT angiogram.

A young man was diagnosed with a rare hair loss condition usually seen in older women.

Woodhouse-Sakati Syndrome can include unique symptoms like liver issues and low growth hormone.

PAON shows skin patterns due to genetic mosaicism.

A black-skinned woman was diagnosed with Vogt-Koyanagi-Harada disease and treated with steroids and eye drops.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

A girl with a rare skin condition improved after one month of treatment with acitretin.