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Yellow and orange colors are important for diagnosing certain skin conditions.

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

Ashy dermatosis may be linked to atopy and thyroid disease and can be treated with topical steroids.

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

Whale genes show changes that help them live in water, like less hair and better flippers.

Graying hair happens due to aging and might be delayed by new treatments.

Some skin problems can be signs of diabetes or other metabolic diseases and recognizing them can help diagnose and treat these diseases early.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

The gene Msx2 is crucial for hair follicle regeneration during wound healing.

Chronic kidney disease can cause skin problems that affect patient quality of life, and treating these conditions can improve outcomes.

Unwanted facial hair significantly impacts over 40% of women's psychological and social well-being, and various treatment options are available.

The document concludes that unruly hair can be congenital or acquired, often lacks specific treatments, and can be managed with oils and short hairstyles.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

Chemotherapy can cause significant hair thinning and changes in hair texture, while tamoxifen has a smaller effect.

Parathyroid hormones are important for hair growth, but their use in treating hair loss from chemotherapy is still uncertain.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Women with AGA have higher lipid levels, increasing heart disease risk.

Treat pattern hair loss with finasteride and topical minoxidil.

Symmetrical Acrokeratoderma (SAK) may be a unique skin condition in China, lacking specific treatment and needing long-term monitoring.

Patients with severe alopecia areata have higher levels of MIF, which decrease after successful treatment.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Carbamazepine may cause reversible nail detachment.

Retinoids can prevent skin cancer in high-risk people but have side effects and require more research on dosing and effectiveness.

New hair loss treatments may include topical medications, injections, and improved transplant methods.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Found different proteins in balding and non-balding cells, giving insight into hair loss causes.