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Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

Loss of keratin K2 causes skin problems and inflammation.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

Psychotropic medications can cause skin reactions, including severe conditions like SJS and TEN, and it's important for psychiatrists to recognize and manage these side effects.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Red spots on fingertips can be a sign of a skin condition linked to gluten sensitivity, treatable with a gluten-free diet.

Eyebrow loss has many causes and requires accurate diagnosis for proper treatment.

Allergic reactions to blood thinners are rare but can be serious, requiring careful management and alternative treatments.

Most Latino farmworkers in the study had skin diseases, with fungal infections being the most common.

Changes in keratin affect skin health and can lead to skin disorders like blistering diseases and psoriasis.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Hormonal treatment is effective for women with acne not helped by usual treatments, especially if they have hormonal imbalances.

Light microscopy is useful for diagnosing different hair disorders.

Topical contact sensitizers can treat certain skin conditions but are rarely used in the U.K.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Systemic retinoids are effective for psoriasis but have side effects; benefits may outweigh risks, especially when reducing cancer risks from other treatments.

Germany recognizes skin cancer from UV exposure as an occupational disease, emphasizing prevention and care for affected workers.

Stopping the medication infliximab and starting new treatments helped a woman's hair grow back and improved her scalp condition.

Using systemic drugs as creams for skin conditions shows promise, but more research is needed to confirm their effectiveness and safety.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Two babies needed surgery to remove hair tightly wrapped around their toes to prevent serious injury.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

Leptin affects skin and hair health and may worsen some skin conditions, but more research is needed to understand its full impact.