Search

everythinglearnresearchcommunity

for

Search:↓

Frontal fibrosing alopecia might be linked to autoimmune diseases.

The symposium highlighted the importance of understanding disease mechanisms for targeted dermatology treatments.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Vitamin D is crucial for skin health and managing skin diseases.

PAON shows skin patterns due to genetic mosaicism.

Systemic lupus erythematosus is a complex autoimmune disease mainly affecting women, with varied symptoms and unknown exact cause.

The document summarizes skin and immune system disease findings, especially related to AIDS, from the 1980s.

Polycystic Ovary Syndrome is linked to higher risk of hypertension and heart disease.

Adult stem cells are effective and ethically acceptable for treating various diseases.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Mesenchymal stromal cell therapies show promise for treating various diseases but need more research and standardization.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

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.

Psoriasis is a common, genetically influenced skin disease worsened by stress and lifestyle, but targeted treatments are promising.

Men have worse COVID-19 outcomes than women due to genetic and hormonal differences.

PCOS is a hereditary disorder that can lead to diabetes and heart disease if not treated early.

Skin problems in the elderly are unique and may indicate other diseases, involving changes in skin, hair, nails, and increased cancer risk.

The document concludes that there have been significant improvements in diagnosing and treating skin diseases, including melanoma, with new techniques and therapies.

TGF-β is crucial for tissue repair and can cause diseases if not properly regulated.

The document concludes that skin biopsies, genetic and environmental factors, and specific treatments are important in managing cutaneous lupus erythematosus.

Metabolic syndrome in kids and teens is linked to obesity and increases diabetes and heart disease risk; early lifestyle changes are crucial for management.

Hirsutism is common body hair growth due to genetics and hormones, and while not a disease, it can be distressing; virilisation includes hirsutism with other male traits and needs medical attention.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

The girl's condition improved with treatment, showing no new autoimmune diseases and hair regrowth.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

Minoxidil and finasteride are the only FDA-approved treatments for hair loss caused by genetic and hormonal factors, but their effectiveness is often doubted, indicating a need for new treatments.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.