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A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

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.

Forensic medicine is crucial for justice and needs continuous innovation and technology integration.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

The dietary supplement significantly improved skin, nails, and hair in older adults.

Finasteride increases hair count and improves hair growth with low risk of side effects.

Male androgenetic alopecia involves hair follicle miniaturization due to DHT, with potential treatments using inhibitors and blockers.

New research has found 14 genes linked to the risk of developing alopecia areata, improving understanding and treatment options.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

Eating disorders are serious, often undiagnosed conditions requiring early treatment, with anorexia being the most deadly and binge-eating the most treatable.

Men with male pattern baldness may not have different hormone levels, but their hair follicles are likely more sensitive to hormones.

Type 2 diabetes in youth is increasing, with high treatment failure rates and more severe than Type 1; certain drugs can lower lipid levels effectively with varying side effects, and apples may benefit heart health like statins but with fewer side effects.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

The textbook "Dermatology" is highly recommended for its comprehensive content, user-friendly design, and extensive visual aids.

Mice treatments didn't grow hair, a patient treatment may affect immune response, and people with hair loss often feel anxious or depressed.

Hair loss can be treated with medications like minoxidil and finasteride or surgery, but treatment effectiveness varies by alopecia type and accurate diagnosis is important.

Men with severe hair loss may have a higher risk of heart disease.

FGF13 gene changes cause excessive hair growth in a rare condition.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

FGF5 gene mutations cause long hair in domestic cats.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

New gene discoveries have improved diagnosis and treatment for skin and hair disorders, but more research is needed to fully understand them.

Forensic DNA Phenotyping accurately predicts physical traits and is used in investigations, but needs more diverse population data for confirmation.

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 woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.