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A woman with systemic sclerosis developed a unique scarring hair loss combining features of systemic sclerosis and frontal fibrosing alopecia.

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

Consider amyloidosis in patients with specific nail changes and check for systemic issues.

Lipedematous alopecia involves a thickened scalp and hair loss, with limited effective treatments available.

Generalized hair follicle hamartoma can occur with systemic lupus erythematosus.

About 8% of people with systemic lupus erythematosus have chronic scarring alopecia, with certain symptoms and positive antibodies increasing the risk, while immunosuppressants may lower it.

A woman on immunosuppressants developed two rare scalp conditions, which improved with specific treatments.

Chronic scarring alopecia is common in SLE patients and needs early detection and management.

Hair restoration greatly improved George's confidence and self-identity.

Women are more likely to have Lichen planopilaris, and treatments with cyclosporine and methotrexate are most effective but less safe than mycophenolate mofetil.

Lichen planus pigmentosus mainly affects middle-aged women with darker skin, is underreported, and is hard to treat.

Misdiagnosis of LPP in AGA patients can cause hair transplant issues.

A patient with Rhupus was diagnosed with Rowell syndrome and treated with various medications.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Lamins are vital for cell survival, organ development, and preventing premature aging.

Lichen planopilaris and frontal fibrosing alopecia are likely the same disease with different clinical appearances.

An 87-year-old man showed unusual signs of Hodgkin lymphoma, primarily high calcium levels, which improved after treatment and revealed the disease.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

These hair loss conditions might be part of a spectrum, not separate issues.

A 5-year-old girl with a rare genetic disorder, lipoid proteinosis, showed reduced new lesions but persistent scars after avoiding skin trauma.

SLE is more common among Nigerians than previously thought, especially in women, requiring early treatment.

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

Sarcoidosis can mimic other skin disorders, making diagnosis challenging.

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

Sympathetic activation and venous tone are crucial for heart failure symptoms.

Different types of hair loss in lupus need careful diagnosis for proper treatment.

Oral lichen planus is not linked to sex hormone levels.

Early diagnosis and genetic counseling are crucial for managing adrenoleukodystrophy.

Vogt-Koyanagi syndrome often leads to partial or complete blindness and responds poorly to treatment.

Leukemia can sometimes appear as unusual skin issues in children.