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RHUPUS should be considered in children with deforming arthritis.

A dog with skin issues improved with prednisone after accurate diagnosis.

Methotrexate is effective and well-tolerated in children for certain skin conditions but requires careful monitoring.

Neonatal lupus symptoms usually resolve, but some children may develop other autoimmune diseases later.

Tofacitinib is a promising treatment for children with rheumatic diseases.

The dog has Color Dilution Alopecia, causing hair loss and increased risk of skin infections.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

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

Some treatments like methotrexate with prednisone might help juvenile morphea, but more research is needed to confirm.

People with Alopecia Areata are more likely to have certain health issues like ulcerative colitis and type 1 diabetes, but less likely to have others like hypertension and type 2 diabetes.

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

Black-tailed deer have four types of pelages and molt twice a year.

A young boy with a rare skin and nail condition improved significantly with simple topical treatments.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Juvenile-onset lupus patients have more severe symptoms and need stronger treatment.

Dogs with skin lesions often have blood abnormalities and damaged hair.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Juvenile dermatomyositis can worsen quickly and needs strong treatment.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A Thai Bangkaew dog with diabetes and pancreatic issues improved with insulin, enzymes, and vitamins.

The study concluded that careful examination is key to differentiate between lipidized fibrous histiocytoma and juvenile xanthogranuloma.

First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

Children with different rheumatologic diseases have specific skin symptoms that can help with diagnosis.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Some young Angus cattle had skin problems due to not enough vitamin A, which got better after they were given more vitamin A.

A 5-year-old girl with a rare skin disorder was effectively treated with skin creams instead of oral medication.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Early diagnosis and treatment of systemic-onset juvenile idiopathic arthritis are crucial for improvement.