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CDH3-related disease causes worsening eye and hair issues.

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

Systemic corticosteroids can cause unusual skin issues in people with juvenile rheumatoid arthritis.

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

Genetic testing confirmed a rare disorder causing hair loss and vision problems in a Saudi family, stressing its importance for diagnosis and counseling.

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

RHUPUS should be considered in children with deforming arthritis.

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

Juvenile dermatomyositis can worsen quickly and needs strong treatment.

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

Low free thyroxine (FT4) is common in young lupus patients and needs quick diagnosis and treatment.

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

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

A new genetic mutation was found causing hair and eye issues in a boy.

Skin symptoms are important for diagnosing and managing juvenile-onset systemic lupus erythematosus and usually get better with treatment.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

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.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

The analyses helped identify different skin diseases in the two dogs.

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

JSLE patients often have more hormone and metabolism issues, so regular check-ups and preventing obesity can help.

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

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

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

A multi-drug treatment can effectively clear extensive calcinosis in juvenile dermatomyositis.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

PFOS exposure disrupts hormone levels and enzyme activities in juvenile frogs, affecting males and females differently.

Mycophenolate mofetil is effective for treating severe lupus nephritis in children.

Ocrelizumab helped control lupus in a pregnant patient, leading to the birth of a healthy baby.