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Changing the environment around stem cells could help tissue repair, but it's hard to be precise and avoid side effects.

Estrogens help reduce skin aging, and SERMs might offer similar benefits without the risks of hormone therapy.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Some vaccines, like the hepatitis B vaccine, might be linked to the hair loss condition Alopecia Areata, but more research is needed.

Psoriasis worsens in winter in India due to less sunlight and dry skin, needing personalized treatment.

These skin conditions in African men need combined medical treatments and lifestyle changes.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

The genetic variant studied does not affect PCOS symptoms in Kashmiri women.

Minoxidil effectively treats female pattern hair loss.

Topical minoxidil helps treat female pattern hair loss, but more research needed for other treatments.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

Some treatments like methotrexate with prednisone might help juvenile morphea, but more research is needed to confirm.

Effective treatments for premature hair graying still require significant research.

New genetic mutations linked to rare skin disorders were found in three newborns.

A man lost all his hair permanently after hepatitis C treatment, a side effect not seen before.

Behçet's Disease may be caused by genetic and environmental factors leading to abnormal immune responses, and stress management and new treatments could improve patient outcomes.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

Current treatments for alopecia show no significant long-term benefits.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

Use antiandrogens and other treatments for hair loss.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

Understanding the immune-related causes of Alopecia Areata has led to potential treatments like JAK inhibitors.

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.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

The research identified key proteins that affect wool fiber thickness in Angora rabbits.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Parents often claim to use more home safety measures than they actually do.