Search

everythinglearnresearchcommunity

for

Search:↓

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

The Oat mouse model shows mild retinal degeneration, useful for testing treatments.

Scarring alopecia involves increased immune cells and specific gene changes near damaged hair follicles.

Most patients with systemic lupus erythematosus in Malwa, India, show skin symptoms like photosensitivity and rashes.

Turner's syndrome may be linked to autoimmune diseases like psoriasis and alopecia areata, needing comprehensive care.

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

Some children with localized scleroderma are rarely resistant to methotrexate, and no common profile for resistance was found.

Graham-Little Piccardi Lassueur Syndrome is a rare skin condition with specific hair loss and skin symptoms.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

Early diagnosis and aggressive treatment of lupus nephritis can prevent kidney damage and improve outcomes.

Patients with RASopathies are at risk for autoimmune disorders and should be routinely screened.

People with polycystic ovary syndrome have worse meibomian gland and ocular surface conditions.

A young woman had a rare skin reaction to a medication for her joint disease, and a combination therapy improved her condition.

High-dose corticosteroid treatment helped improve symptoms in a patient with Adult Onset Still Disease.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

A mouse model for studying scleroderma in chronic graft-versus-host disease was successfully created.

Serenoa repens may cause long-lasting sexual and psychiatric side effects.

Removing SIX1 in fat cells reduces skin fibrosis.

Elderly SLE patients show fewer typical symptoms and more hormonal side effects.

The study found that skin inflammation and immune response pathways are activated in Solar Urticaria patients after UV exposure, unlike in healthy people.

Some patients with mycosis fungoides or Sézary syndrome experience hair loss, which may be similar to alopecia areata or linked to skin lesions, possibly due to abnormal T cells, and bexarotene can help treat it.

Unique fat cells near fibrotic areas contribute to systemic sclerosis progression.

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.

Herpes simplex virus infections should be considered in pemphigus patients to avoid unnecessary changes in treatment.

Tph cells are linked to the severity of systemic lupus erythematosus.

Myositis in lupus patients is linked to skin rash, hair loss, blood issues, and high disease activity.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

A 12-year-old boy in rural south India had a rare skin condition causing hair loss and inability to sweat.

It's unclear if COVID-19 vaccination causes SLE; more research is needed.