Search

everythinglearnresearchcommunity

for

Search:↓

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Insulin resistance is linked to many health problems and is influenced by diet, genetics, and other factors.

Seaweeds have beneficial compounds for skin care, including anti-aging and protective effects.

Budesonide is not effective for maintaining remission in Crohn's disease beyond three months.

No single treatment is clearly effective for central serous chorioretinopathy.

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

Topical corticosteroids are the best initial treatment for children's alopecia areata.

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

Treating H. pylori infection might help cure alopecia areata.

Tailored treatments for alopecia areata are recommended based on severity and patient needs.

Laser hair removal is popular for long-term hair reduction but carries risks, requiring well-trained operators and better regulations, especially in South Africa.

Some steroid-induced health issues in rodents improved after stopping treatment, but hair loss and eye problems did not.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Alopecia areata can be managed with various treatments, and severe cases should be referred to dermatologists.

Acyzol could help treat conditions caused by zinc deficiency.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Caspases are enzymes important for both cell death and various non-lethal cell functions, affecting head development and hair growth, with different caspases playing specific roles.

Purslane has many health benefits and potential uses in medicine, food, and farming.

Minoxidil nanoparticles significantly boost hair growth in mice compared to regular minoxidil.

Hair microscopy is a simple and cost-effective method to help diagnose systemic diseases in children.

VKHD and sarcoidosis may share a common cause.

Long COVID is a serious, long-lasting illness that needs more recognition and support.

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

Obesity leads to physical, metabolic, reproductive issues, higher healthcare costs, and mental health problems.

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

Glucocorticoids for progressive muscular dystrophy in children don't improve muscle strength or function but do increase certain side effects.

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

Tamsulosin increases the risk of floppy iris during eye surgery.

Standardized procedures are crucial for collecting and preparing biological samples to ensure accurate clinical metabolomics results.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.