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Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

An 82-year-old man's white hair regained color after taking etretinate for psoriasis.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

Ulcerative sarcoidosis in body folds is rare and improved with prednisone and hydroxychloroquine.

Argentine-cross polo ponies commonly develop sarcoid tumors with distinct types and histopathological features.

Vitamin D supplements should be used cautiously in sarcoidosis patients, with regular monitoring to avoid high calcium levels.

Ichthyoses are skin disorders causing scales, with treatment depending on type and severity.

Sarcoidosis can cause severe high calcium levels, hair loss, and kidney failure.

A rare scalp condition causing hair loss improved with a specific cream.

Orange spots in scalp trichoscopy can help diagnose scalp sarcoidosis.

Patients with ichthyosis often experience symptoms similar to psoriasis and atopic dermatitis, suggesting that targeted therapies could improve their condition.

Sarcoidosis can cause scarring hair loss on the scalp, which is rare.

Scalp sarcoidosis can cause hair loss and needs accurate diagnosis and treatment with specific medications.

Sarcoidosis can mimic other skin disorders, making diagnosis challenging.

Two boys had a rare skin condition needing to be differentiated from similar disorders, with unclear inheritance due to few cases.

If someone has scaly skin, muscle stiffness, and intellectual disability, doctors should consider Sjogren-Larsson Syndrome, but other conditions if more symptoms are present.

Early diagnosis and thorough evaluation are crucial for better outcomes in alopecic sarcoidosis.

VKHD and sarcoidosis may share a common cause.

Skin problems after waxing led to a sarcoidosis diagnosis.

The text talks about a rare skin condition causing hair loss and suggests that people with this should also check their lung and heart health.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

A Holstein calf in Iran with a severe genetic skin disorder was euthanized due to incurable symptoms.

The four patients have a unique type of ichthyosis affecting hair follicles.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

Removing a tumor may resolve associated skin and hair symptoms.

A woman's skin and hair conditions improved after her cancerous tumor was removed.

Treatment with moisturizers improved the skin condition of a girl with a rare genetic skin disorder.