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The top research priorities for congenital ichthyosis include long-term side effects of oral retinoids, best topical treatments, and treatments for itch and hair loss.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

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

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

A baby with a skin condition improved with treatment but developed a rare form of the condition affecting only his trunk.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Surgery on a baby with a skin disorder improved eyelid position and eye health.

Removing a tumor may resolve associated skin and hair symptoms.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

A new gene mutation linked to a skin condition was found in a Spanish family.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

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

Gluconolactone products can significantly reduce skin scaling in golden retrievers with ARCI.

Hypertrichosis (excessive hair growth) can help diagnose superficial epidermolytic ichthyosis.

Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.

Some scalp sores are linked to different inherited skin conditions.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

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

Vitamin D3 is important for bone health and may help treat various diseases beyond bone-related conditions.

Triparanol therapy can cause hair loss and skin dryness without inflammation or damage to hair follicles or skin structures.

Mutations in keratin genes cause cell fragility and various skin disorders.

Retinoids can help treat skin disorders by improving the skin's outer layer.

Oral retinoids are effective for treating severe skin disorders but have reversible side effects and risks for pregnant women.

A boy with Sjogren-Larsson syndrome has skin and muscle symptoms due to a specific enzyme deficiency.

FoxN1 overexpression in young mice harms immune cell and skin development.

Symmetrical Acrokeratoderma (SAK) may be a unique skin condition in China, lacking specific treatment and needing long-term monitoring.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Most skin conditions in Down syndrome are benign and involve dry or thickened skin.