Search

everythinglearnresearchcommunity

for

Search:↓

Diagnosing alopecia areata is challenging and requires careful examination and various tests to distinguish it from other hair loss types.

Docetaxel, a chemotherapy drug, was reported to cause psoriasis in a patient for the first time.

Alopecia areata causes sudden hair loss, has genetic links, and can be managed but not cured.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

Alopecia areata causes patchy hair loss and involves immune system disruptions.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

A 45-year-old woman with autoimmune diseases experienced patchy hair loss due to alopecia areata, which has no cure but can be treated, with varying success.

Understanding drug effects and careful monitoring are crucial for safe and effective dermatology treatments.

Alopecia areata in infants may be more common than previously thought.

Topical corticosteroid treatment showed no significant difference from placebo in treating alopecia areata in children.

Alopecia areata is a genetic and immune-related hair loss condition that is often associated with other autoimmune diseases and does not typically cause permanent damage to hair follicles.

Patients with certain skin diseases are willing to spend significant time on treatment, indicating a high impact on their lives and a need for better treatments.

Recognizing specific skin features helps diagnose and manage lupus erythematosus effectively.

Alopecia areata is an autoimmune disease causing hair loss, treatable with immune-modulating drugs, and linked to genetics.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

Simvastatin/ezetimibe may help some patients with severe alopecia areata regrow hair.

Sequential therapy with dupilumab and baricitinib improved hair regrowth and atopic dermatitis in a child without adverse reactions.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

A mix of methotrexate, corticosteroids, and topical minoxidil effectively treated severe total body hair loss, but caused stretch marks and needs long-term monitoring.

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

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Adults should not consume more than 255 micrograms of selenium per day to avoid risk of hair loss and other side effects.

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

K42 and K124 keratins are only found in horse hoof lamellae.

Hair microscopy is a simple and cost-effective method to help diagnose systemic diseases in children.

Understanding the cause of bitemporal hair loss is key to deciding the right treatment.

Higher CD70 and CD27 gene expression in alopecia areata lesions predicts disease severity and activity.

Hair loss, known as Androgenetic Alopecia, is often caused by hormones and can be diagnosed using noninvasive techniques. Treatments include topical minoxidil and oral finasteride, with new treatments being explored. There may also be a link between this type of hair loss and heart disease risk.

Environmental pollutants can damage hair health and cause hair loss.