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Targeting the Smoothened receptor shows promise for treating certain cancers.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Understanding genetic mutations helps diagnose and treat skin disorders like ichthyosis.

The most common causes of hair loss in Jordanian children are fungal infections, autoimmune hair loss, and hair shedding after fever, with zinc deficiency also being a notable cause.

Dermatologists found teledermatology useful and confidence-boosting for diagnosing skin conditions, but faced limitations like technical issues and prescription restrictions. Despite this, they saw its potential to improve access to skin care, especially in remote areas.

Tissue expansion is an effective treatment for certain types of hair loss, providing immediate coverage with hair-bearing skin.

Vitiligo is underreported in medical claims and is linked to certain skin types and autoimmune diseases.

Break dancing on the head may cause a type of scarring hair loss that needs early treatment to prevent permanent damage.

Alopecia mucinosa can be treated successfully with minocycline.

The document concludes that fexofenadine reduces inflammation in chronic hives, cholestyramine helps half of pregnant women with itchy rashes, and relaxing incisions are a good alternative in facial surgery for the elderly.

Taking 1 mg of finasteride daily could potentially treat rare hair conditions like Acquired Progressive Kinking of the Hair and whisker hair.

External factors can cause skin cancer cells that usually don't spread to grow and form tumors in mice.

Hair follicles have a more inactive cell cycle than other skin cells, which may help develop targeted therapies for skin diseases and cancer.

Mesotherapy might improve hair growth, but more research is needed to confirm its safety and effectiveness.

A substance called miR-1246 may help treat severe hair loss by reducing certain immune cell activities.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

The conference concluded with plans for joint research into children's skin conditions and emphasized the importance of collaboration and patient-focused research.

The number of dermatologists in the US increased from 1995 to 2011, but they were unevenly distributed, mainly in urban areas, and areas with higher income and education levels.

Patients with nonmelanoma skin cancers are most bothered by fear of progression, appearance concerns, and having cancer.

The book "Eye and Skin Disease" is recommended for its detailed coverage of the connection between eye and skin conditions.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

The most common causes of hair loss in children in South-East Nigeria are fungal infections and alopecia areata.

The article concludes that hair loss is a common side effect of drugs treating skin cancer by blocking the hedgehog pathway, but treatment should continue, and more selective drugs might prevent this side effect.

Different types of scarring alopecia may be stages of one disease, and accurate diagnosis is crucial to prevent permanent hair loss.

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Ischemic modified albumin could be a new indicator of oxidative stress in people with alopecia areata.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

WNT signaling is crucial for skin development and healing.