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The study found that polymorphous light eruption varies among patients and can be distinguished from benign summer light eruption by the time it takes for symptoms to appear after sun exposure.

Women with PCOS have more insulin resistance and are more likely to have heart-related health issues, with insulin resistance being a bigger factor than β-cell problems.

The document concludes that various findings in rheumatology offer insights into disease severity, treatment responses, and potential risks in medication, with some limitations due to unspecified participant numbers.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Microbes might play a role in vitiligo.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

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.

Diagnosing and treating skin conditions is challenging, especially when drug reactions mimic other diseases.

Rheumatology clinics should always provide preconception counseling for women on DMARDs.

A new model can predict drug-disease links well, helping drug research.

Zebrafish are useful for studying and developing treatments for human skin diseases.

Latisse (bimatoprost 0.03%) is widely used in dermatology but the document doesn't give detailed evidence or numbers.

PCOS is a complex condition in women that can lead to health issues, and lifestyle changes are the best management approach.

No single treatment is clearly effective for central serous chorioretinopathy.

Mycophenolate mofetil may improve lupus nephritis remission more than cyclophosphamide but with uncertain safety.

Diabetes causes lasting cell dysfunctions, leading to serious complications even after blood sugar is controlled.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

New materials that better mimic natural skin structure could improve healing, especially for chronic wounds.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

A new mutation in the HR gene causes hair loss in a specific family.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Monilethrix causes short, fragile hair with no specific treatment available.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Hair loss in children is diagnosed and treated differently than in adults, with different common causes and a focus on less invasive methods.

Trichoscopy helps diagnose hair and scalp problems but isn't always definitive and should be used with other methods.

Alopecia Areata is an autoimmune condition causing hair loss, influenced by genetics, environment, and possibly improved by anti-MIF therapy, with many patients experiencing regrowth within a year.