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Hepatitis B virus exposure may be linked to increased risk of alopecia areata.

Oxygen levels can drop during liver transplant if bypass pressures are too high, but other reasons should be checked first.

Knockout mice showed anemia and hair loss, suggesting other ways exist for iron absorption.

Two cases showed skin abnormalities without bone or neural defects.

Visceral leishmaniasis can mimic rheumatoid arthritis symptoms, especially in immunocompromised patients.

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

Splenic eumelanin in C57BL/6 mice is different from hair eumelanin.

Secukinumab treatment may cause HBV reactivation and hair discoloration.

Hidradenitis suppurativa may be more severe in people with Mediterranean fever gene mutations.

A man lost all his hair permanently after hepatitis C treatment, a side effect not seen before.

Congenital adrenal hyperplasia may be linked to adrenal myelolipoma.

A rare skin growth in a baby was successfully removed without coming back.

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

Hair follicle stem cell transplants can reverse liver cirrhosis by blocking harmful cell activation.

A woman in Sri Lanka was diagnosed with lupus after presenting with protein loss from the gut and other symptoms.

CD8+ T cells play a key role in graft-versus-host disease in certain mice models.

Bullous pemphigoid, intrahepatic cholangiocarcinoma, and alopecia areata may share immune-related causes.

Juvenile dermatomyositis can worsen quickly and needs strong treatment.

cGVHD often severely affects the skin, causing rapid aging and other issues.

A rare skin infection in a 10-year-old kidney transplant patient was successfully managed by adjusting medication.

A woman's liver was damaged by taking the herbal supplement Shou-Wu-Pian, but it got better after she stopped using it.

A man with both skin lesions and lung cancer improved quickly with chemotherapy, suggesting the skin condition might be a reaction to immune system injury.

The muscle damage was caused by T-cell large granular lymphocytic leukemia, not dermatomyositis.

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

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

The boy's scurvy symptoms improved with vitamin C treatment, highlighting the need for a balanced diet.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

Erythropoietin overexpression disrupts hair growth and fat formation in mice.

Children with Parry Romberg Syndrome had successful facial fat-grafting surgeries after disease stabilization with no complications.

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