Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

A patient with advanced kidney cancer and no hepatitis C developed skin inflammation due to a drug called interferon alpha-2a.

Discoid lupus erythematosus can be mistaken for a skin infection, complicating diagnosis and treatment.

Lykoi cats' unique sparse hair is linked to specific genetic variants in the Hairless gene.

A 13-year-old girl was diagnosed with juvenile lupus, showing only hair loss as a symptom.

Taiwan reported its first case of a rare scalp condition with no clear cause or treatment.

Rhupus is a complex syndrome that is hard to diagnose due to unclear clinical criteria.

Early referral to a pediatric rheumatologist and thorough evaluation are crucial for treating complex overlap syndromes effectively.

Children with alopecia areata, especially with Down syndrome or thyroid issues, should be screened for thyroid disease.

Antigen presenting cells around hair follicles are crucial in SLE-related hair loss.

Rituximab effectively managed a difficult case of juvenile lupus with complications, reducing the need for steroids.

Patients with lichen planus should be tested for hepatitis C.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

Some people with lichen planus pigmentosus might later develop frontal fibrosing alopecia.

LC-OCT is an effective new method for diagnosing classic lichen planopilaris.

A 64-year-old man had a rare skin cancer near his ear, unresponsive to antibiotics, with specific skin and hair follicle changes.

A kidney transplant patient developed leprosy, likely due to immunosuppression and genetic factors, and improved with treatment.

People with atopic dermatitis have more CD4+ T cells that respond to a certain bacterial lipid, which may play a role in the skin condition's inflammation.

A 5-year-old boy's skin condition improved with systemic valganciclovir after a cardiac transplant and immunosuppressive therapy.

Anti-Ku-positive patients often have muscle weakness and autophagy plays a key role in their condition.

Alopecia areata patients have more activated T cells in their blood, which may help in developing treatments.

Cathepsin L deficiency causes large, abnormal cell structures and health issues in mice.

Alopecia is common in lupus patients, causing significant anxiety and is linked to the disease itself.

A 61-year-old Filipino man had a skin condition that looked like another disease, making diagnosis difficult.

ILC1-like cells can cause alopecia areata by themselves.

The patient's symptoms improved with treatment but recurred when the steroid dose was reduced, requiring ongoing therapy.

Doctors should consider comedonic discoid lupus erythematosus to avoid misdiagnosis.

Frequent blood transfusions in beta thalassemia can lead to thyroid problems.

Ossification in trichilemmal cysts is more common than previously believed.