Search

everythinglearnresearchcommunity

for

Search:↓

Vitiligo causes white skin patches, often starts before age 20, and is linked to other health issues.

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.

PCOS in teens is hard to diagnose, linked to genetics and lifestyle, and managed with weight loss and medication.

People with alopecia areata often have lower levels of vitamin D, zinc, and folate, but more research is needed to understand if supplements can help treat it.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Some people experience severe, long-lasting side effects from fluoroquinolone antibiotics, leading to the recommendation of limited use and increased awareness of these risks.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

Oxidative stress contributes to hair graying and loss as we age.

New treatments targeting specific genes show promise for treating keratin disorders.

Hair ages due to genetics and environmental factors, leading to graying and thinning, with treatments available for some conditions.

The document concludes that accurate diagnosis and personalized treatment are important for skin problems in women with PCOS.

Products should be called 'sperm-safe' only after thorough, well-designed tests.

AMH helps estimate ovarian reserve but doesn't predict pregnancy chances; age is more important.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

Looking at skin can help find and treat serious diseases early.

The document concludes that hair analysis is not good for assessing nutrition but can detect long-term heavy metal exposure.

Hair ages due to various factors and treatments like minoxidil and finasteride can help, but more research and better public awareness are needed.

Foxp3 is crucial for regulatory T cell function, and targeting these cells may help treat immune disorders.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

JAK inhibitors like tofacitinib may effectively treat Alopecia Areata.

Self-amplifying RNA could be a better option for protein replacement therapy with lower doses and lasting effects, but delivering it into cells is still challenging.

Growth factors greatly affect hair loss, with different levels seen in men, women, younger patients, and at the start of the condition.

Men with baldness, ear creases, and hairy ears have a higher risk of heart disease.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Tiger cubs fed artificial milk lacking certain amino acids developed eye problems and hair loss.

HYDRO DELUXE BIO hyaluronic acid hydrogel is compatible with skin cells, may reduce inflammation, promote blood vessel growth, and protect against oxidative stress, suggesting it could help revitalize hair follicles.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.