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A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Ritlecitinib is effective and safe for treating severe alopecia areata in people aged 12 and older.

Hair turning darker can be a sign of skin cancer.

A 2-year-old girl with a rare vitamin D disorder had rickets and hair loss, but treatment was ineffective due to poor compliance.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Ixekizumab may be an effective first treatment for a rare skin condition causing hair loss.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

Applying a specific inhibitor lightens skin and hair color.

Dihydroxyacetone in self-tanning lotion helped reduce sun-related skin issues in a woman with variegate porphyria.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

A missing mK6irs1 gene causes hair loss in mice.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Human skin responds to light with protective mechanisms, but more research is needed to understand these processes and their implications for health and therapy.

Infants with severe KID syndrome may be more prone to serious infections and need close monitoring.

Spironolactone helps reduce fluid in the eye in Central Serous Chorioretinopathy, but doesn't improve vision and recurrence is common.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Upadacitinib may effectively treat resistant lichen planopilaris.

Early recognition and treatment of VATS in transplant patients improve outcomes.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Higher activity in lichen planopilaris is linked to certain immune and tissue genes.

Managing frontal fibrosing alopecia and lichen planus pigmentosus is challenging due to resistant hair loss and skin discoloration.

A 19-year-old with MRKHS developed complete hair loss, and treatment options were discussed.

Hydroxypinacolone retinoate is a potent anti-aging ingredient for skin that is more effective and less irritating than other forms of retinoids.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

Lichen planopilaris should be considered when diagnosing hair loss in people with darker skin as it may be often missed.