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Seaweeds contain beneficial compounds with potential uses in food, cosmetics, and health, but more research is needed to improve extraction and safety.

Stem cell therapy is promising for treating various health conditions, but more research is needed to understand its full potential and address challenges.

A specific gene mutation causes Olmsted syndrome.

Skin cysts might help advance stem cell treatments to repair skin.

A girl with Evans' syndrome had her low platelet count successfully treated with zanubrutinib.

Fat-derived stem cells show promise for treating skin issues and improving wound healing, but more research is needed to confirm the best way to use them.

Understanding how acne develops in different diseases could lead to new treatments.

Cronkhite-Canada syndrome is rare, has a poor prognosis, and requires early diagnosis and ongoing treatment.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

Scientists have improved 3D models of human skin for research and medical uses, but still face challenges in perfectly replicating real skin.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

PCOS is managed by lifestyle changes and personalized medication to improve symptoms and fertility.

Some lesser-known causes of PCOS include autoimmune issues, genetic mutations, and changes in the body's microbiome.

The conference concluded with plans for joint research into children's skin conditions and emphasized the importance of collaboration and patient-focused research.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

The true incidence of post-Finasteride syndrome is unclear, and more research is needed.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

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.

Intermediate filaments are crucial for cell differentiation and stem cell function.

Taking too much vitamin E caused a young man's blood clotting problems, which improved after he stopped the vitamin E and got treatment.

Myotonic Dystrophy may age cells faster, and drugs that target aging could be potential treatments.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

Premature aging increases the risk of immune problems and autoimmune diseases.

More research is needed to understand the genetic causes of Alopecia areata to develop better treatments.

A new mouse model for vitiligo helps study immune responses and potential treatments.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Ashwagandha root improved symptoms of nonclassic 11-hydroxylase deficiency in an elderly woman.

Zinc, copper, and iron are important for skin health and may help diagnose skin diseases.