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Hair shaft disorders are diagnosed through examination and history, with general care and some treatments offering improvement.

Juvenile alopecia areata is more severe and has a worse prognosis than maturity-onset alopecia areata.

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

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

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

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.

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.

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

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.

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.

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.

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

Tofacitinib can cause skin eruptions similar to palmoplantar pustulosis.

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.

A gene mutation in mice causes skin defects and early death.