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New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

Cytochrome P-450 enzymes in the skin help break down various substances and could be targeted to treat skin conditions.

A rare skin disorder, Ichthyosis with confetti, has no cure but treatment focuses on managing symptoms with moisturizers.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Near-infrared laser therapy with Indocyanine Green dye improves acne by reducing inflammation without side effects.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

People with early psychosis eat more calories, saturated fat, and sugar, and the drug olanzapine may lead to eating even more calories.

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

Some teenagers with anorexia nervosa have worse cognitive abilities, especially in visual and spatial tasks, and this is more common in those with a lower body weight.

RY-023, a specific drug, can improve early stage memory learning without affecting general activity in rats, but it's less effective for later learning stages and doesn't impact memory recall.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Stress can cause hair loss by negatively affecting hair follicles and this effect might be reversed with specific treatments.

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

Substance P may worsen acne by increasing inflammation, but corticosteroids might help by reducing this effect.

17-β-Estradiol applied to the skin stops hair growth, while ICI 182 780 helps hair grow in mice.

Icariin helps mouse hair grow by boosting a growth factor in skin cells.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Guasha changed rat skin appearance and blood vessels temporarily without affecting certain nerve proteins or fiber structure.

A cross-bred lamb with severe skin and movement issues had ichthyosis fetalis but normal vitamin A levels.

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

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

TCDD speeds up skin barrier formation by increasing certain gene expressions.

Nanoparticles can improve skin drug delivery but have challenges like toxicity and stability that need more research.

New compounds with carborane showed anti-androgen effects similar to flutamide.

Asian hair is generally straight and thick, with unique disorders and properties, and more research is needed to understand it fully.

Certain medications and patient factors increase the risk of Intraoperative Floppy Iris Syndrome during cataract surgery, but with careful planning and technique adjustments, complications can be minimized.

Minoxidil nanoparticles can potentially be a more effective treatment for hair growth than current treatments.

The nanoparticles improved hair growth and enlarged hair bulbs.