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Acitretin is effective for severe psoriasis and can be used long-term due to no immunosuppression, but must be carefully monitored for side effects and is not for pregnant women.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

Fox genes are important for hair growth and development in cashmere goats.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

The conclusion is that a combination of noninvasive treatments and lifestyle changes can improve skin health during menopause.

Animal research has greatly advanced dermatology.

People with alopecia areata have a higher risk of depression and anxiety, and often face unemployment and work absences.

Hair loss can indicate underlying systemic diseases and addressing these can sometimes reverse the hair loss.

The document concludes that identifying the cause of eyebrow and eyelash loss is key to treating it and improving quality of life.

UVA1-light therapy successfully treated a child's skin condition, mycosis fungoides.

Early recognition and treatment of atypical alopecia areata in infants are crucial.

Doctors should diagnose hair loss by examining the patient and possibly doing tests, and then treat it based on the type, which may prevent permanent hair loss.

The document concludes that early diagnosis and treatment are key for pediatric hair loss disorders, and addressing the emotional effects on children is important.

Early diagnosis and treatment are crucial for preventing permanent hair loss in various scalp conditions, and while new treatments are promising, more research is needed to evaluate their effectiveness.

The document concludes that Cutaneous Lupus Erythematosus has different forms, is influenced by genetic and environmental factors, and can be treated with various medications, but more targeted therapies are needed.

ESR2 gene linked to female-pattern hair loss.

Foxn1 gene regulation is crucial for thymus development but not for hair growth.

The representation of skin conditions in medical reviews partly matches their real-world impact.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

The skin's layers protect, sense, and regulate the body's internal balance, but can be prone to cancer.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Platelet-rich plasma treatment is not very effective for chronic severe alopecia areata.

Dermatologists play a key role in identifying and documenting signs of abuse and injury for forensic investigations.

Keratin proteins are crucial for healthy skin, but mutations can cause skin disorders with no effective treatments yet.

Skin aging is caused by stem cell damage and can potentially be delayed with treatments like antioxidants and stem cell therapy.

PCOS in teen girls should be managed with lifestyle changes and sometimes medication to improve symptoms and health.

Gendered social factors, not just biology, contribute to sex differences in adverse drug events.

Skin problems are common in lupus, often appearing first, with various types and treatments, and careful monitoring is important for diagnosis and management.

The document concludes that Functional Hypothalamic Amenorrhea should be carefully diagnosed and managed to prevent health complications, using lifestyle changes and specific medications.

Fish oil increased cell growth and macrophages in the skin but didn't affect COX-2 expression.