Search

everythinglearnresearchcommunity

for

Search:↓

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

Acyzol could help treat conditions caused by zinc deficiency.

Acitretin is effective for severe skin conditions but has significant side effects and requires careful monitoring.

Non-biologic immunosuppressive drugs are crucial for treating autoimmune and chronic inflammatory skin diseases.

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.

Early treatment of acne is crucial to prevent scarring and psychological effects.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

Covers common skin issues in kids, their diagnosis, treatment, and need for specialist care.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Some chemicals absorbed through the skin can cause serious health problems.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

Eating too much selenium can cause bad breath, hair loss, and nail changes, with harmful effects starting at low daily doses.

Some treatments can stabilize Frontal Fibrosing Alopecia, but more research is needed to find effective treatments, and hair transplants often fail.

Bariatric surgery may help severely obese teenagers but has risks and requires careful patient selection and long-term care.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

A small forehead lesion led to the discovery of a significant brain arteriovenous malformation in a young girl.

The WNT signaling pathway is important in many diseases and targeting it could offer new treatments.

More high-quality research is needed to recommend flavonoids and saponins for clinical use.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Teriflunomide is effective and generally safe for treating relapsing-remitting multiple sclerosis.

MRI helps distinguish between pituitary adenomas and craniopharyngiomas, guides treatment for pediatric CNS tumors, and assesses rhinocerebral mucormycosis with a high mortality rate in transplanted patients.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

The document is a detailed medical reference on skin and genetic disorders.